Original source

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

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

Chromosome 22:50568712 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

22:g.50568712G>T

About this variant

This variant overlaps 10 transcripts.

Variant displays