rs2078085499
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800839
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2461C>T (p.Leu821Phe)
Allele
T
Clinical Significance
Likely pathogenic