rs777212434
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
20
Location
10299331
Variant Type
SNP
Genes
ClinVar
Name
NM_130811.4(SNAP25):c.471C>T (p.Ile157=)
Allele
T
Clinical Significance
Likely benign