rs34614566
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
9
Location
110800724
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2346G>T (p.Glu782Asp)
Allele
T
Clinical Significance
Uncertain significance