rs779401827
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800862
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2484C>T (p.Pro828=)
Allele
T
Clinical Significance
Likely benign