Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.39 (A)
Location

Chromosome 12:112443538 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59099219, rs36112025

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2514 individual genotypes.

Variation displays