Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.02 (A)
Location

Chromosome 10:49608074 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.49608074G>A

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays