rs903123754
- 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
C
Alternative Allele
A
G
Chromosome
9
Location
110762350
Variant Type
SNP
Genes
LOC107987115
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.920+142C>A
Allele
A
Clinical Significance
Likely benign