rs760793449
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
110787710
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1799A>G (p.Tyr600Cys)
Allele
G
Clinical Significance
Uncertain significance