rs368395413
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
9
Location
110775821
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1218C>T (p.Cys406=)
Allele
T
Clinical Significance
Likely benign