Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.13 (G)
Location

Chromosome 10:49607650 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.49607650A>G

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3919 sample genotypes.

Variant displays