rs1447190013
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
110800889
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2511A>G (p.Leu837=)
Allele
G
Clinical Significance
Likely benign