rs1001603852
- Likely benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
G
Alternative Allele
A
Chromosome
19
Location
7629831
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001171155.2(PET100):c.-3G>A
Allele
A
Clinical Significance
Likely benign