Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.14 (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

Variation displays