Original source

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

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

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