rs756096336
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
9
Location
110785683
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1743C>A (p.Ile581=)
Allele
A
Clinical Significance
Likely benign