Variant report

Variant	rs10220698
Chromosome Location	chr14:63385634-63385635
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]
rs10136789	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10146437	0.91[CEU][hapmap];1.00[JPT][hapmap]
rs10150703	0.85[CEU][hapmap]
rs11158460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12590790	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1543436	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1956011	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs1956013	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs1956014	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs28608483	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][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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