Variant report

Variant	rs12071464
Chromosome Location	chr1:211392863-211392864
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11581409	0.86[ASN][1000 genomes]
rs2095752	0.99[ASN][1000 genomes]
rs2095753	0.82[ASN][1000 genomes]
rs3111245	0.99[ASN][1000 genomes]
rs3111246	0.82[ASN][1000 genomes]
rs3125832	0.80[ASN][1000 genomes]
rs3125833	0.99[ASN][1000 genomes]
rs55758006	0.96[EUR][1000 genomes]
rs56381832	0.96[EUR][1000 genomes]
rs57331968	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs61850977	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61850980	0.96[EUR][1000 genomes]
rs61850982	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7522532	0.94[EUR][1000 genomes]
rs7523875	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3340221	chr1:211391629-211393677	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3337898	chr1:211392229-211393277	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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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