rs2064354640
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
20
Location
10306145
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.569C>T (p.Thr190Ile)
Allele
T
Clinical Significance
Uncertain significance