rs1238400476
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110800543
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2165T>C (p.Val722Ala)
Allele
C
Clinical Significance
Uncertain significance