Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 12:106357492 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.106357492T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays