rs760339630
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
20
Location
10275538
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.47G>A (p.Arg16Gln)
Allele
A
Clinical Significance
Uncertain significance