rs2077898173
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110787706
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1795C>T (p.Pro599Ser)
Allele
T
Clinical Significance
Uncertain significance