Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 12:90964283 (forward strand) | View in location tab

Co-located

with COSMIC COSM4045347 (A/G)

Most severe consequence

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 262 individual genotypes.

Variation displays