Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 22:50584590 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts.

Variant displays