rs2030995839
- Uncertain significance
Your Genotype
Sign InDescription
This variant was classified as: Uncertain significance. The available evidence on this variant's pathogenicity is insufficient or conflicting. The following ACMG criteria were applied in classifying this variant: PM2.
Reference Allele
C
Alternative Allele
A
Chromosome
19
Location
7620076
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020196.3(XAB2):c.2267-1G>T
Allele
A
Clinical Significance
Uncertain significance