ClinVar Miner

List of variants in gene NPHP4 reported as not provided by GenomeConnect - Invitae Patient Insights Network

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015102.5(NPHP4):c.3175G>A (p.Ala1059Thr)	rs202004152	0.00024
NM_015102.5(NPHP4):c.3721G>A (p.Val1241Ile)	rs535789951	0.00002

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