rs199811263
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
G
Chromosome
9
Location
110800329
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1951A>C (p.Met651Leu)
Allele
C
Clinical Significance
Likely benign