rs577931355
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800489
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2111G>A (p.Cys704Tyr)
Allele
A
Clinical Significance
Likely benign