Original source

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

Alleles
G/C/T|Ancestral: C|Ambiguity code: B|MAF: 0.48 (C)
Location

Chromosome 9:123365221 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays