Variant report

Variant	rs16922097
Chromosome Location	chr10:22500944-22500945
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10508641	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs12263070	1.00[CEU][hapmap]
rs16922008	1.00[CEU][hapmap]
rs56186224	0.87[AMR][1000 genomes]
rs56264992	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812745	0.87[AMR][1000 genomes]
rs72812756	0.87[AMR][1000 genomes]
rs72812784	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812786	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812789	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812790	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812794	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812795	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812799	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72814804	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72814806	1.00[EUR][1000 genomes]
rs72814808	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72814811	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72814816	1.00[EUR][1000 genomes]

No data

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

No data

Quick Search:

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

what's new

Quick links