rs776545636
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
9
Location
110785013
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1583A>C (p.Lys528Thr)
Allele
C
Clinical Significance
Uncertain significance