Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome 12:32790861 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3186128

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

About this variant

This variant overlaps 5 transcripts and has 2506 individual genotypes.

Variation displays