rs369015815
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110775926
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1323T>C (p.His441=)
Allele
C
Clinical Significance
Likely benign