Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.26 (C)
Location

Chromosome 9:117580914 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60118116

HGVS name

9:g.117580914C>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays