Variant report

Variant	rs10190016
Chromosome Location	chr2:191262713-191262714
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10170897	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10202825	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208045	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs13390311	0.93[ASN][1000 genomes]
rs13409203	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs16832573	0.90[CHB][hapmap]
rs34121676	0.84[ASN][1000 genomes]
rs35151949	0.84[EUR][1000 genomes]
rs35253896	1.00[EUR][1000 genomes]
rs36015572	0.82[ASN][1000 genomes]
rs3811610	0.91[CHB][hapmap];1.00[JPT][hapmap]
rs73048070	0.96[ASN][1000 genomes]
rs73050047	1.00[ASN][1000 genomes]

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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