Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.06 (T)

Chromosome 16:67977964 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs56991233

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts and has 4078 sample genotypes.

Variant displays