Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.50 (A)
Location

Chromosome 9:125235313 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2604 sample genotypes and is mentioned in 3 citations.

Variant displays