List of variants in gene JPH2 reported as likely benign by Clinical Genetics, Academic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020433.5(JPH2):c.572C>G (p.Pro191Arg)	rs554853074	0.00048
NM_020433.5(JPH2):c.1204G>A (p.Glu402Lys)	rs147407445	0.00038
NM_020433.5(JPH2):c.1852A>G (p.Thr618Ala)	rs376612687	0.00017
NM_020433.5(JPH2):c.820G>A (p.Asp274Asn)	rs376694047	0.00002

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