rs1161007370
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110787809
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1898T>C (p.Phe633Ser)
Allele
C
Clinical Significance
Uncertain significance