rs1161905783
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110784895
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1465T>C (p.Ser489Pro)
Allele
C
Clinical Significance
Uncertain significance