Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H|MAF: 0.35 (T)
Location

Chromosome 22:35070492 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17830251, rs57990740

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

Variant displays