Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:58155985 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.58155985C>T

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays