rs930182416
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110775841
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1238T>C (p.Met413Thr)
Allele
C
Clinical Significance
Uncertain significance