Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.15 (A)
Location

Chromosome 12:71938373 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR073562

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56853432

HGVS name

12:g.71938373T>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 2510 sample genotypes and is mentioned in 36 citations.

Variant displays