rs775509048
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800775
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2397C>T (p.Gly799=)
Allele
T
Clinical Significance
Uncertain significance