RS267606919 NPHS1

Health Risk Chr 19:35831056
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What This Variant Does
"CLNSIG=5
Associated Conditions
Finnish congenital nephrotic syndrome
Nephrotic syndrome
Inborn genetic diseases
Finnish congenital nephrotic syndrome
Nephrotic syndrome
Inborn genetic diseases
Other Variants in NPHS1
rs1973075631 rs1972884983 rs1972875644 rs2527606158 rs28939695 rs267606917 rs267606918 rs139954720 rs386833861 rs386833863
Ask Dr. Hemsworth about this variant