Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs58915468

HGVS name

2:g.236165176G>A

About this variant

This variant overlaps 5 transcripts and has 2508 individual genotypes.

Variation displays