rs1588014706
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
110767889
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.990A>G (p.Ala330=)
Allele
G
Clinical Significance
Likely benign