Original source

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

Alleles
C/-|Ancestral: C|MAF: 0.01 (-)
Location

Chromosome 22:37125606 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

22:g.37125606delC

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays