rs387906803
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
9
Location
110767930
Variant Type
SNP
Genes
LOC107987115
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.1031C>G (p.Pro344Arg)
Allele
G
Clinical Significance
Pathogenic