rs781462535
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
9
Location
110762218
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.920+10T>C
Allele
C
Clinical Significance
Likely benign