rs4989078
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
G
Chromosome
9
Location
113211764
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_015258.2(FKBP15):c.54-172A>C
Allele
G
Clinical Significance
Benign
T
A
G
9
113211764
SNP
NM_015258.2(FKBP15):c.54-172A>C
G
Benign