rs770373727
- Uncertain significance
Your Genotype
Sign InDescription
Has not been previously published as pathogenic or benign to our knowledge
Reference Allele
C
Alternative Allele
G
Chromosome
9
Location
110800586
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2208C>G (p.Asn736Lys)
Allele
G
Clinical Significance
Uncertain significance