rs1588037378
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110784840
Variant Type
SNP
Genes
LOC107987115
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.1410G>A (p.Lys470=)
Allele
A
Clinical Significance
Likely benign