RS869312915 NPHP3

Health Risk Chr 3:132699418
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Nephronophthisis
Inborn genetic diseases
Nephronophthisis
Other Variants in NPHP3
rs119456959 rs119456960 rs119456961 rs119456962 rs119456963 rs119456964 rs754508002 rs267606916 rs142021049 rs145643112
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