List of variants in gene JPH2 reported as benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 10

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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.2073T>C (p.Phe691=)	rs6093935	0.33656
NM_020433.5(JPH2):c.1728C>G (p.Pro576=)	rs74352869	0.21684
NM_020433.5(JPH2):c.1186G>A (p.Ala396Thr)	rs3810510	0.20153
NM_020433.5(JPH2):c.1179C>T (p.His393=)	rs7268512	0.08199
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.380-6C>T	rs201197277	0.00218
NM_020433.5(JPH2):c.1424G>A (p.Arg475His)	rs765754956	0.00079
NM_020433.5(JPH2):c.783G>C (p.Ala261=)	rs201085317	0.00033

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