Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
Evidence status

HGVS name

8:g.48917403G>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

Variant displays