Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 6:111407233 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.111407233C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ImmunoChip

Variation displays