Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 10:99531610 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.99531610C>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts and has 2508 individual genotypes.

Variation displays