Variants in gene JPH2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_020433.5(JPH2):c.637C>T (p.Arg213Trp)	rs767328866	0.00145
NM_020433.5(JPH2):c.128A>G (p.Asn43Ser)	rs138992849	0.00072
NM_020433.5(JPH2):c.572C>G (p.Pro191Arg)	rs554853074	0.00048
NM_020433.5(JPH2):c.1380G>A (p.Ala460=)	rs531877510	0.00044
NM_020433.5(JPH2):c.1204G>A (p.Glu402Lys)	rs147407445	0.00038
NM_020433.5(JPH2):c.1015G>A (p.Gly339Ser)	rs368290474	0.00035
NM_020433.5(JPH2):c.1852A>G (p.Thr618Ala)	rs376612687	0.00017
NM_020433.5(JPH2):c.1729G>A (p.Glu577Lys)	rs181096982	0.00001
NM_020433.5(JPH2):c.838G>A (p.Glu280Lys)	rs748282723	0.00001
NM_020433.5(JPH2):c.1375G>A (p.Ala459Thr)
NM_020433.5(JPH2):c.1674G>A (p.Pro558=)
NM_020433.5(JPH2):c.624C>G (p.Ala208=)	rs398124358

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