RS28939695 NPHS1

Health Risk Chr 19:35848142
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What This Variant Does
"[OMIM:NEPHROSIS 1, CONGENITAL, FINNISH TYPE]
Associated Conditions
Proteinuria
Finnish congenital nephrotic syndrome
Congenital nephrotic syndrome
Focal segmental glomerulosclerosis
Proteinuria
Finnish congenital nephrotic syndrome
Congenital nephrotic syndrome
Focal segmental glomerulosclerosis
Other Variants in NPHS1
rs1973075631 rs1972884983 rs1972875644 rs2527606158 rs267606919 rs267606917 rs267606918 rs139954720 rs386833861 rs386833863
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