List of variants in gene PREPL reported as benign by GeneDx

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001171613.2(PREPL):c.1479+117C>T	rs10183231	0.99267
NM_001171613.2(PREPL):c.889-160G>A	rs10185647	0.96562
NM_001171613.2(PREPL):c.-48-129A>G	rs698764	0.71988
NM_001171613.2(PREPL):c.1087-47A>G	rs2033951	0.71897
NM_001171613.2(PREPL):c.1629+111T>C	rs2053454	0.67659
NM_001171613.2(PREPL):c.349+108G>A	rs17580226	0.67538
NM_001171613.2(PREPL):c.-48-142C>A	rs698765	0.67513
NM_001171613.2(PREPL):c.888+43T>A	rs2289463	0.67293
NM_001171613.2(PREPL):c.143-128_143-126del	rs35987136	0.64958
NM_001171613.2(PREPL):c.349+80G>T	rs12053381	0.64667
NM_001171613.2(PREPL):c.1629+168G>A	rs2053455	0.63478
NM_001171613.2(PREPL):c.485+228A>T	rs2304770	0.62162
NM_001171613.2(PREPL):c.888+197C>T	rs4953092	0.61386
NM_001171613.2(PREPL):c.1480-121T>G	rs12474294	0.08254
NM_001171613.2(PREPL):c.76-124C>T	rs17498312	0.06154
NM_001171613.2(PREPL):c.486-191C>G	rs75339650	0.04964
NM_001171613.2(PREPL):c.143-19C>T	rs10514790	0.04940
NM_001171613.2(PREPL):c.888+167A>G	rs17032140	0.04934
NM_001171613.2(PREPL):c.-49+1898A>G	rs77060839	0.04787
NM_001171613.2(PREPL):c.1753+135T>C	rs77212913	0.04397
NM_001171613.2(PREPL):c.225T>A (p.Ala75=)	rs72875319	0.03485
NM_001171613.2(PREPL):c.143-185G>A	rs72875321	0.02715
NM_001171613.2(PREPL):c.350-173A>G	rs6752523	0.01939
NM_001171613.2(PREPL):c.-48-95C>G	rs698763
NM_001171613.2(PREPL):c.-48-95C>T	rs698763
NM_001171613.2(PREPL):c.350-12_350-10del	rs61004197
NM_001171613.2(PREPL):c.350-49del	rs11421998
NM_001171613.2(PREPL):c.350-63dup	rs11421998
NM_001171613.2(PREPL):c.485+82C>T	rs2304769
NM_001171613.2(PREPL):c.75+134_75+139del	rs148666471

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