rs34267283
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110787796
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1885C>T (p.Leu629Phe)
Allele
T
Clinical Significance
Likely benign