List of variants in gene NPHP4 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_015102.5(NPHP4):c.2542C>T (p.Arg848Trp)	rs17472401	0.01606
NM_015102.5(NPHP4):c.3479C>T (p.Pro1160Leu)	rs113445782	0.01143
NM_015102.5(NPHP4):c.1852G>A (p.Glu618Lys)	rs571655	0.01009
NM_015102.5(NPHP4):c.4237G>A (p.Asp1413Asn)	rs115910810	0.00328

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