rs781506865
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
9
Location
110800627
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.2249T>A (p.Ile750Asn)
Allele
A
Clinical Significance
Uncertain significance