rs376635652
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
110800578
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2200G>A (p.Gly734Ser)
Allele
A
Clinical Significance
Uncertain significance