rs74633160
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
111578960
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001146108.2(PTGR1):c.496-9T>C
Allele
G
Clinical Significance
Benign
A
G
9
111578960
SNP
NM_001146108.2(PTGR1):c.496-9T>C
G
Benign