Original source

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

Alleles
C/A/G|Ancestral: G|Ambiguity code: V|MAF: 0.48 (G)
Location

Chromosome 22:36358158 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

Variant displays