rs2078084758
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
9
Location
110800818
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2440T>G (p.Tyr814Asp)
Allele
G
Clinical Significance
Uncertain significance