Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.03 (G)

Chromosome 12:55452989 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs74092332

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts and has 2506 sample genotypes.

Variant displays