Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 12:52796199 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17371344, rs56834715

HGVS name

12:g.52796199A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays