rs115758301
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
111570132
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001146108.2(PTGR1):c.838C>T (p.Arg280Cys)
Allele
A
Clinical Significance
Likely benign