rs1292312575
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
9
Location
110787776
Variant Type
SNP
Genes
ClinVar
Name
NM_005592.4(MUSK):c.1865A>T (p.Asp622Val)
Allele
T
Clinical Significance
Uncertain significance