List of variants in gene JPH2 reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020433.5(JPH2):c.421T>C (p.Tyr141His)	rs387906897	0.00001
NM_020433.5(JPH2):c.1213G>T (p.Ala405Ser)	rs557878787
NM_020433.5(JPH2):c.424G>T (p.Gly142Ter)	rs765874503

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