Variant report

Variant	rs11762051
Chromosome Location	chr7:121937298-121937299
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11761299	0.86[CHB][hapmap]
rs11767283	0.81[CHB][hapmap];1.00[MEX][hapmap];0.82[AMR][1000 genomes]
rs11978249	0.84[ASN][1000 genomes]
rs1443753	0.81[CHB][hapmap]
rs1867335	0.81[CHB][hapmap]
rs1909945	0.99[ASN][1000 genomes]
rs5007345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs538558	0.86[CHB][hapmap]
rs58938116	0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6968786	0.86[CHB][hapmap]

No data

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

No data

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Input of quick search could be:

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

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