Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.30 (G)
Location

Chromosome 19:10289628 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs827787, rs61116170, rs3760652

HGVS name

19:g.10289628G>A

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature, has 3766 sample genotypes and is mentioned in 2 citations.

Variant displays