Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:26785970 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.26785970G>A

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts and has 2 individual genotypes.

Variation displays