rs779710805
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
9
Location
110800978
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2600T>C (p.Val867Ala)
Allele
C
Clinical Significance
Uncertain significance