Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.38 (T)
Location

Chromosome 12:90963572 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58781624, rs17251134

HGVS name

12:g.90963572T>G

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 transcript and has 3764 sample genotypes.

Variant displays