rs2064355285
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
20
Location
10306167
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_130811.4(SNAP25):c.591A>C (p.Gln197His)
Allele
C
Clinical Significance
Uncertain significance