List of variants in gene PLCE1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_016341.4(PLCE1):c.2999G>A (p.Ser1000Asn)	rs61751498	0.00200
NM_016341.4(PLCE1):c.1567A>G (p.Ile523Val)	rs61751494	0.00188
NM_016341.4(PLCE1):c.2076A>T (p.Thr692=)	rs147203844	0.00155
NM_016341.4(PLCE1):c.642A>T (p.Gly214=)	rs149064632	0.00110
NM_016341.4(PLCE1):c.513G>A (p.Val171=)	rs61749239	0.00101
NM_016341.4(PLCE1):c.2214+7C>T	rs201418194	0.00042
NM_016341.4(PLCE1):c.1651T>C (p.Leu551=)
NM_016341.4(PLCE1):c.1927G>T (p.Ala643Ser)	rs61886330
NM_016341.4(PLCE1):c.2598G>C (p.Thr866=)	rs368426208

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