List of variants in gene NPHP1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001128178.3(NPHP1):c.232T>C (p.Tyr78His)	rs140446520	0.00127
NM_001128178.3(NPHP1):c.104A>G (p.Glu35Gly)	rs368025611	0.00003
NM_001128178.3(NPHP1):c.460G>A (p.Gly154Ser)	rs769509705	0.00002
NM_001128178.3(NPHP1):c.1513T>C (p.Ser505Pro)	rs903701752	0.00001
NM_001128178.3(NPHP1):c.1522G>C (p.Val508Leu)	rs573192954
NM_001128178.3(NPHP1):c.635AAG[5] (p.Glu215dup)	rs777677768

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