rs1600775326
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
20
Location
10293217
Variant Type
SNP
Genes
ClinVar
Name
NM_130811.4(SNAP25):c.220G>A (p.Ala74Thr)
Allele
A
Clinical Significance
Uncertain significance