RS199506378 NPHS2

Health Risk Chr 1:179551435
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What This Variant Does
"CLNSIG=4
Associated Conditions
Nephrotic syndrome
type 2
Idiopathic nephrotic syndrome
Inborn genetic diseases
Nephrotic syndrome
type 2
Idiopathic nephrotic syndrome
Inborn genetic diseases
Other Variants in NPHS2
rs878853214 rs878853215 rs878853213 rs878853216 rs878853212 rs878853211 rs74315343 rs2526380257 rs74315346 rs74315347
Ask Dr. Hemsworth about this variant