rs374078491
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
9
Location
110787717
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1806T>G (p.Pro602=)
Allele
G
Clinical Significance
Likely benign