Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.16 (A)
Location

Chromosome 12:51186924 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs52826536

HGVS name

12:g.51186924C>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

Variant displays