rs181652070
- Uncertain significance
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
9
Location
110787758
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1847C>T (p.Ser616Leu)
Allele
T
Clinical Significance
Uncertain significance
Name
NM_005592.4(MUSK):c.1847C>G (p.Ser616Trp)
Allele
G
Clinical Significance
Uncertain significance