Variant report

Variant	rs7555722
Chromosome Location	chr1:179399253-179399254
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 126 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10913739	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10913752	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10913753	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10913755	0.93[ASN][1000 genomes]
rs10913760	0.93[ASN][1000 genomes]
rs10913761	0.93[ASN][1000 genomes]
rs10913762	0.93[ASN][1000 genomes]
rs10913766	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs10913767	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs10913768	0.93[ASN][1000 genomes]
rs10913769	1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs10913770	0.93[ASN][1000 genomes]
rs10913771	0.93[ASN][1000 genomes]
rs10913809	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11577579	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs11578241	0.93[ASN][1000 genomes]
rs11581659	0.81[EUR][1000 genomes]
rs11582158	0.84[CEU][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs11582255	0.93[ASN][1000 genomes]
rs11582293	0.93[ASN][1000 genomes]
rs11582754	0.93[ASN][1000 genomes]
rs11586744	1.00[ASN][1000 genomes]
rs11801919	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11802624	0.93[ASN][1000 genomes]
rs11802625	0.93[ASN][1000 genomes]
rs11802637	0.93[ASN][1000 genomes]
rs11803938	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs11807559	1.00[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs11811198	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12401957	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs12403933	0.84[CEU][hapmap]
rs12408443	1.00[ASN][1000 genomes]
rs12409337	1.00[ASN][1000 genomes]
rs12722736	1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs12724320	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12724496	0.93[ASN][1000 genomes]
rs12724525	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs12724634	0.93[ASN][1000 genomes]
rs12724778	1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs12724901	0.84[CEU][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs12725414	0.93[ASN][1000 genomes]
rs12726506	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12726875	0.93[ASN][1000 genomes]
rs12729067	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12729775	0.93[ASN][1000 genomes]
rs12729788	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12730056	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12736279	0.80[ASN][1000 genomes]
rs12736545	0.80[ASN][1000 genomes]
rs12738262	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs12738929	0.93[ASN][1000 genomes]
rs12739116	0.93[ASN][1000 genomes]
rs12741425	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12743018	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12743585	0.86[ASN][1000 genomes]
rs12744251	0.93[ASN][1000 genomes]
rs12744438	0.93[ASN][1000 genomes]
rs12744949	1.00[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs12744976	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12746253	0.93[ASN][1000 genomes]
rs12746331	0.86[EUR][1000 genomes]
rs12746578	1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs12747626	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12749461	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12750591	0.93[ASN][1000 genomes]
rs12751260	0.93[ASN][1000 genomes]
rs12751550	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12753162	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12753310	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs12755634	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12755804	0.85[EUR][1000 genomes]
rs12756624	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12757708	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12757910	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12757935	1.00[ASN][1000 genomes]
rs12758415	1.00[ASN][1000 genomes]
rs12758828	0.84[CEU][hapmap];0.81[JPT][hapmap]
rs12760048	1.00[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs12760534	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs1328597	0.80[ASN][1000 genomes]
rs1328598	0.80[ASN][1000 genomes]
rs1410589	0.80[ASN][1000 genomes]
rs1576224	0.82[AMR][1000 genomes]
rs2209919	0.80[ASN][1000 genomes]
rs34291276	0.80[ASN][1000 genomes]
rs34315375	0.89[EUR][1000 genomes]
rs34463289	0.80[ASN][1000 genomes]
rs35401719	0.80[ASN][1000 genomes]
rs35427395	0.80[ASN][1000 genomes]
rs35978436	0.84[EUR][1000 genomes]
rs3935240	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[YRI][hapmap]
rs4130266	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs4233177	0.93[ASN][1000 genomes]
rs4233178	0.93[ASN][1000 genomes]
rs4233179	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs4261076	0.84[EUR][1000 genomes]
rs4360491	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4418554	1.00[ASN][1000 genomes]
rs4454499	0.93[ASN][1000 genomes]
rs4651028	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs4651037	0.85[AMR][1000 genomes]
rs4652368	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4652383	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs61821011	0.93[ASN][1000 genomes]
rs61826364	0.80[ASN][1000 genomes]
rs61826365	0.80[ASN][1000 genomes]
rs6425536	0.82[EUR][1000 genomes]
rs6666939	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs7513782	1.00[ASN][1000 genomes]
rs7513973	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7521106	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7524128	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs7532155	0.93[ASN][1000 genomes]
rs7550638	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[YRI][hapmap]
rs7551894	1.00[ASN][1000 genomes]
rs7554103	0.88[JPT][hapmap];1.00[ASN][1000 genomes]
rs7555895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9662026	1.00[ASN][1000 genomes]
rs9699789	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3514400	chr1:179349344-179400533	Enhancers Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3514401	chr1:179349344-179400533	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3451112	chr1:179352344-179400533	Enhancers ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1819329	chr1:179371973-179442337	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv466217	chr1:179371973-179477921	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv548297	chr1:179371973-179477921	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv548298	chr1:179376896-179436288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7555722	AXDND1	cis	Thyroid	GTEx

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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