Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.21 (-)
Location

Chromosome 16:23181011 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23181011delG

About this variant

This variant overlaps 1 transcript and has 2506 individual genotypes.

Variation displays