rs200030321
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
20
Location
10299394
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.534C>T (p.Ile178=)
Allele
T
Clinical Significance
Likely benign