rs1011593420
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
9
Location
110800895
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2517G>C (p.Trp839Cys)
Allele
C
Clinical Significance
Uncertain significance