rs1555794286
- Pathogenic
Your Genotype
Sign InDescription
This variant was identified as de novo (maternity and paternity confirmed).
Reference Allele
T
Alternative Allele
A
Chromosome
20
Location
10293197
Variant Type
SNP
Genes
ClinVar
Name
NM_130811.4(SNAP25):c.200T>A (p.Ile67Asn)
Allele
A
Clinical Significance
Pathogenic