Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.07 (G)
Location

Chromosome 2:118848809 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386619813, rs3806498

HGVS name

2:g.118848809G>A

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3959 sample genotypes.

Variant displays