rs147866099
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
20
Location
10277687
Variant Type
SNP
Genes
ClinVar
Name
NM_130811.4(SNAP25):c.75G>T (p.Ser25=)
Allele
T
Clinical Significance
Benign
G
A
T
20
10277687
SNP
NM_130811.4(SNAP25):c.75G>T (p.Ser25=)
T
Benign