rs1600807788
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
20
Location
10306129
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.553G>C (p.Ala185Pro)
Allele
C
Clinical Significance
Likely pathogenic