Variant report

Variant	rs17422684
Chromosome Location	chr7:104261141-104261142
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10953436	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11764816	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12666704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2193206	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs2193209	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2216243	0.83[CHB][hapmap]
rs6948818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs6974889	1.00[CEU][hapmap];0.80[CHB][hapmap];0.86[JPT][hapmap];0.84[YRI][hapmap]
rs7785650	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9640682	0.83[CHB][hapmap]
rs9641335	1.00[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.83[YRI][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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