rs758777519
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110767962
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1063G>A (p.Ala355Thr)
Allele
A
Clinical Significance
Uncertain significance