List of variants in gene JPH2 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_020433.5(JPH2):c.156C>T (p.Tyr52=)	rs1883790	0.86681
NM_020433.5(JPH2):c.1728C>G (p.Pro576=)	rs74352869	0.21684
NM_020433.5(JPH2):c.1289-7C>T	rs116986535	0.02048
NM_020433.5(JPH2):c.1513G>A (p.Gly505Ser)	rs140740776	0.01021
NM_020433.5(JPH2):c.380-9C>G	rs111987307	0.00419
NM_020433.5(JPH2):c.380-6C>T	rs201197277	0.00218
NM_020433.5(JPH2):c.1971G>A (p.Glu657=)	rs142333841	0.00099

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