rs117661715
- 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
C
Alternative Allele
A
G
T
Chromosome
19
Location
7631533
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001171155.2(PET100):c.199C>T (p.Arg67Cys)
Allele
T
Clinical Significance
Benign