Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:48917403 (forward strand) | View in location tab

Most severe consequence
HGVS name

8:g.48917403G>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts.

Variation displays