Original source

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

A/C/G | Ambiguity code: V | MAF: 0.34 (A)

Chromosome 6:32642980 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2517 sample genotypes.

Variant displays