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
 
Downstream gene variant
HGVS name

8:g.48917403G>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts and 1 regulatory feature.

Variant displays