rs756877019
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
9
Location
110800760
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2382G>C (p.Glu794Asp)
Allele
C
Clinical Significance
Likely pathogenic