rs764142979
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
T
Chromosome
9
Location
110767937
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1038G>C (p.Glu346Asp)
Allele
C
Clinical Significance
Uncertain significance