rs1206244035
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800322
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1944G>A (p.Gly648=)
Allele
A
Clinical Significance
Likely benign