Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.40 (G)
Location

Chromosome 16:57541163 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57492751

HGVS name

16:g.57541163G>A

About this variant

Variant displays