Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs52826536

HGVS name

12:g.51186924C>A

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3692 individual genotypes.

Variation displays