RS386833871 NPHS1

Health Risk Chr 19:35848672
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Finnish congenital nephrotic syndrome
Finnish congenital nephrotic syndrome
Other Variants in NPHS1
rs1973075631 rs1972884983 rs1972875644 rs2527606158 rs28939695 rs267606919 rs267606917 rs267606918 rs139954720 rs386833862
Ask Dr. Hemsworth about this variant