rs371689428
- 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
Chromosome
9
Location
110800885
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2507G>A (p.Arg836His)
Allele
A
Clinical Significance
Uncertain significance