Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.03 (C)
Location

Chromosome 10:71963879 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.71963879G>C

Genotyping chips

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

About this variant

This variant overlaps 2 transcripts and has 2570 individual genotypes.

Variation displays