rs546916589
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
9
Location
110785707
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1767G>C (p.Val589=)
Allele
C
Clinical Significance
Likely benign