rs1588025437
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
110775827
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1224A>G (p.Lys408=)
Allele
G
Clinical Significance
Uncertain significance