rs2997742
- 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
1
Location
115717983
Variant Type
SNP
Genes
ClinVar
Name
NM_001232.4(CASQ2):c.784-89C>T
Allele
A
Clinical Significance
Benign