Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.37 (A)
Location

Chromosome 10:49607466 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17719152, rs58882174

HGVS name

10:g.49607466G>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4029 sample genotypes and is mentioned in 3 citations.

Variant displays