List of variants in gene NPHP4 reported as uncertain significance for Renal dysplasia and retinal aplasia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015102.4(NPHP4):c.-235G>A	rs765435500	0.00058
NM_015102.4(NPHP4):c.-236C>T	rs185912310	0.00022
NM_015102.4(NPHP4):c.-225G>A	rs886046469	0.00001
NM_015102.4(NPHP4):c.-237G>C	rs867788720	0.00001

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