List of variants in gene combination NPHP3, NPHP3-ACAD11 reported as benign for Meckel syndrome

Minimum submission review status:		Collection method:
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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_153240.5(NPHP3):c.3759G>A (p.Leu1253=)	rs6794496	0.13621
NM_153240.5(NPHP3):c.2610G>A (p.Pro870=)	rs16839515	0.04323
NM_153240.5(NPHP3):c.*657C>T	rs79224795	0.03141
NM_153240.5(NPHP3):c.3125+7dup	rs11396595

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