RS121907899 NPHP1

Health Risk Chr 2:110163048
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Nephronophthisis 1
Nephronophthisis
NPHP1-related disorder
Inborn genetic diseases
Senior-Loken syndrome 1
Joubert syndrome with renal defect
Retinal dystrophy
Ovarian serous cystadenocarcinoma
Clear cell carcinoma of kidney
Nephronophthisis 1
Nephronophthisis
NPHP1-related disorder
Inborn genetic diseases
Senior-Loken syndrome 1
Joubert syndrome with renal defect
Other Variants in NPHP1
rs1233478832 rs121907898 rs398123285 rs398123286 rs189320299 rs200118387 rs140446520 rs371112962 rs794726975 rs151204566
Ask Dr. Hemsworth about this variant