Variant report

Variant	rs7349788
Chromosome Location	chr5:40634375-40634376
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10035697	0.85[ASN][1000 genomes]
rs10038251	0.85[ASN][1000 genomes]
rs10038367	0.83[ASN][1000 genomes]
rs10040364	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10043839	0.84[ASN][1000 genomes]
rs10043891	0.85[ASN][1000 genomes]
rs10044538	0.85[ASN][1000 genomes]
rs10053469	0.85[ASN][1000 genomes]
rs10055624	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10056173	0.85[ASN][1000 genomes]
rs10057182	0.85[ASN][1000 genomes]
rs10063818	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10063864	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10064394	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10065482	0.85[ASN][1000 genomes]
rs10065874	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10065894	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10068069	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10071117	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10071870	0.85[ASN][1000 genomes]
rs10073344	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10473206	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10473209	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10473210	0.85[ASN][1000 genomes]
rs10473211	0.85[ASN][1000 genomes]
rs10473214	0.82[ASN][1000 genomes]
rs10941521	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10941522	0.85[ASN][1000 genomes]
rs11744569	0.85[ASN][1000 genomes]
rs11744700	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11745462	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11745901	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11949581	0.85[ASN][1000 genomes]
rs11952914	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11955037	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12188666	0.84[ASN][1000 genomes]
rs12513529	0.85[ASN][1000 genomes]
rs1395082	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1553578	0.82[ASN][1000 genomes]
rs1553579	0.85[ASN][1000 genomes]
rs17238368	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28820606	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28862949	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35693860	0.87[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs4599576	0.81[ASN][1000 genomes]
rs4957333	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4957334	0.85[ASN][1000 genomes]
rs4957336	0.85[ASN][1000 genomes]
rs4957337	0.85[ASN][1000 genomes]
rs4957338	0.85[ASN][1000 genomes]
rs4957339	0.85[ASN][1000 genomes]
rs62356461	0.85[ASN][1000 genomes]
rs62358056	0.81[ASN][1000 genomes]
rs62358796	0.85[ASN][1000 genomes]
rs62358800	0.83[ASN][1000 genomes]
rs6860233	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6867169	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879155	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879329	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6892451	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72747928	0.85[ASN][1000 genomes]
rs72747930	0.85[ASN][1000 genomes]
rs72747940	0.85[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7714305	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7726047	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7729332	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9292784	0.83[ASN][1000 genomes]
rs9292785	0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880993	chr5:40521648-40682550	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7349788	RPL37	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:40634200-40634600	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr5:40634200-40635000	Enhancers	Primary T cells fromperipheralblood	blood
3	chr5:40634200-40635400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links