Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/- | Ancestral: T | MAF: 0.39 (-)
Location

Chromosome 22:36353774 (forward strand) | View in location tab

Co-located

with dbSNP rs369816888 (T/C)

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

Variant displays