rs1416891382
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
9
Location
110747762
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.875T>G (p.Phe292Cys)
Allele
G
Clinical Significance
Uncertain significance