Original source

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

Alleles
G/A|Ambiguity code: R|MAF: 0.12 (A)
Location

Chromosome 6:32642972 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays