Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (C)
Location

Chromosome 12:53187150 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17371302, rs60480248

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays