List of variants in gene PLCE1 reported as likely benign for Nephrotic syndrome, type 3

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_016341.4(PLCE1):c.5669C>T (p.Pro1890Leu)	rs58539480	0.01296
NM_016341.4(PLCE1):c.4059C>T (p.Phe1353=)	rs61751499	0.00977
NM_016341.4(PLCE1):c.-287G>A	rs17506379	0.00415
NM_016341.4(PLCE1):c.-165T>C	rs183919560	0.00397
NM_016341.4(PLCE1):c.2728G>A (p.Val910Ile)	rs61751497	0.00284
NM_016341.4(PLCE1):c.2428A>G (p.Ile810Val)	rs78217273	0.00251
NM_016341.4(PLCE1):c.-47A>G	rs11187771	0.00223
NM_016341.4(PLCE1):c.2157C>T (p.Gly719=)	rs200164874	0.00208
NM_016341.4(PLCE1):c.1495C>T (p.Arg499Cys)	rs61751493	0.00134
NM_016341.4(PLCE1):c.2352C>T (p.Asp784=)	rs201793869	0.00044
NM_016341.4(PLCE1):c.-160G>A	rs186468483	0.00029
NM_016341.4(PLCE1):c.1313T>C (p.Val438Ala)	rs199689540	0.00010
NM_016341.4(PLCE1):c.3303C>T (p.Asp1101=)	rs773286585	0.00009
NM_016341.4(PLCE1):c.5979T>C (p.Ser1993=)	rs200943442	0.00009
NM_016341.4(PLCE1):c.1228G>A (p.Glu410Lys)	rs145451189	0.00006
NM_016341.4(PLCE1):c.5670G>A (p.Pro1890=)	rs370864800	0.00002
NM_016341.4(PLCE1):c.1185G>A (p.Leu395=)	rs762259865
NM_016341.4(PLCE1):c.5168-6G>C	rs148239915

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