Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:53189983 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17371344, rs56834715

HGVS name

12:g.53189983A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays