rs1600791112
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
20
Location
10299363
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.503G>A (p.Gly168Asp)
Allele
A
Clinical Significance
Uncertain significance