rs779042240
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800392
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2014C>T (p.Pro672Ser)
Allele
T
Clinical Significance
Uncertain significance