rs1588042433
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
9
Location
110787795
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.1884C>A (p.Ala628=)
Allele
A
Clinical Significance
Likely benign