Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.10 (G)
Location

Chromosome 22:50584723 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs52814495

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays