rs754976866
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800717
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2339C>T (p.Thr780Ile)
Allele
T
Clinical Significance
Uncertain significance