rs1057518966
- Likely pathogenic
Your Genotype
Sign InDescription
This variant was classified as: Likely pathogenic.
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800743
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2365G>A (p.Gly789Ser)
Allele
A
Clinical Significance
Likely pathogenic