Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: < 0.01 (C)
Location

Chromosome 22:31950775 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60502909

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays