rs10817455
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
G
Chromosome
9
Location
113194438
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_015258.2(FKBP15):c.865-269A>T
Allele
A
Clinical Significance
Benign
T
A
C
G
9
113194438
SNP
NM_015258.2(FKBP15):c.865-269A>T
A
Benign