Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 9:124964439 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.124964439C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays