rs2078085552
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
110800840
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005592.4(MUSK):c.2462T>C (p.Leu821Pro)
Allele
C
Clinical Significance
Uncertain significance