Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.24 (G)
Location

Chromosome 12:52468346 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17101314, rs57316766

HGVS name

12:g.52468346A>G

About this variant

This variant overlaps 3 transcripts and has 2578 sample genotypes.

Variant displays