Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.05 (G)
Location

Chromosome 10:68987296 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.68987296T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays