rs766640370
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110787726
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.1815G>A (p.Met605Ile)
Allele
A
Clinical Significance
Pathogenic