Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 10:111075401 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.111075401A>G

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript, has 2617 individual genotypes and is mentioned in 2 citations.

Variation displays