List of variants in gene NPHP1 reported as pathogenic by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001128178.3(NPHP1):c.859G>A (p.Gly287Arg)	rs121907899	0.00012
GRCh37/hg19 2q13(chr2:110881237-110963848)x1
NM_001128178.3(NPHP1):c.555dup (p.Pro186fs)	rs766524637

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