Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.23 (G)
Location

Chromosome 3:171027131 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR052438

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

3:g.171027131T>G

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3523 sample genotypes and is mentioned in 4 citations.

Variant displays