Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.12 (T)
Location

Chromosome 14:64805691 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.64805691C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5

Variation displays