rs2078086619
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110800879
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2501T>C (p.Leu834Pro)
Allele
C
Clinical Significance
Uncertain significance