Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.24 (C)
Location

Chromosome 9:114818634 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60118116

HGVS name

9:g.114818634C>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant has 2778 individual genotypes and is mentioned in 9 citations.

Variation displays