rs74566954
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
2
Location
219239841
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001286423.2(GLB1L):c.722-8T>A
Allele
T
Clinical Significance
Benign
A
T
2
219239841
SNP
NM_001286423.2(GLB1L):c.722-8T>A
T
Benign