rs779231840
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
110785693
Variant Type
SNP
Genes
LOC107987115
ClinVar
Name
NM_005592.4(MUSK):c.1753G>C (p.Ala585Pro)
Allele
C
Clinical Significance
Uncertain significance