rs1057522682
- 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
C
Chromosome
19
Location
7629815
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001171155.2(PET100):c.-19G>C
Allele
C
Clinical Significance
Likely benign