rs397515450
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
110800558
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2180C>T (p.Ala727Val)
Allele
T
Clinical Significance
Pathogenic