Original source

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

Alleles
A/C/G|Ancestral: A|Ambiguity code: V|MAF: 0.03 (G)
Location

Chromosome 12:55452989 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs74092332

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 10 transcripts and has 2506 sample genotypes.

Variant displays