Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.02 (T)
Location

Chromosome 12:53183028 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58116199

HGVS name

12:g.53183028C>T

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Illumina_1M-duo, Illumina_HumanOmni5

Variation displays