Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.39 (A)
Location

Chromosome 2:236165176 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58915468

HGVS name

2:g.236165176G>A

About this variant

This variant overlaps 5 transcripts and has 2508 sample genotypes.

Variant displays