rs758777089
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
T
Chromosome
9
Location
110787724
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1813A>T (p.Met605Leu)
Allele
T
Clinical Significance
Uncertain significance