Variant report

Variant	rs9640682
Chromosome Location	chr7:104246719-104246720
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10487220	0.90[CEU][hapmap];0.83[GIH][hapmap];0.90[MEX][hapmap];0.88[TSI][hapmap]
rs11764816	0.82[CHB][hapmap]
rs12154499	0.94[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs12666704	0.83[CHB][hapmap]
rs17422684	0.83[CHB][hapmap]
rs2193206	0.82[CHB][hapmap]
rs2193209	0.84[CHB][hapmap]
rs2216243	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2216244	0.94[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];0.86[ASN][1000 genomes]
rs2891730	0.90[MEX][hapmap]
rs4730031	0.94[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.90[MEX][hapmap];0.86[ASN][1000 genomes]
rs6948818	0.83[CHB][hapmap]
rs73181811	0.86[ASN][1000 genomes]
rs7785650	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs9640680	1.00[CEU][hapmap];0.91[CHB][hapmap];0.92[JPT][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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