rs1568623929
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
20
Location
10293007
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.164-154C>A
Allele
A
Clinical Significance
Uncertain significance