Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.25 (A)
Location

Chromosome 13:48232374 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

13:g.48232374G>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

Variant displays