Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

with HGMD-PUBLIC CR073562

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56853432

HGVS name

12:g.71938373T>A

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 2510 individual genotypes and is mentioned in 35 citations.

Variation displays