List of variants in gene LRP2 reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.2603C>G (p.Thr868Ser)	rs150752263	0.00100
NM_004525.3(LRP2):c.6858T>A (p.Phe2286Leu)	rs140918583	0.00089
NM_004525.3(LRP2):c.6938C>T (p.Pro2313Leu)	rs73035708	0.00069
NM_004525.3(LRP2):c.2063G>A (p.Arg688His)	rs148943767	0.00010
NM_004525.3(LRP2):c.10704G>A (p.Pro3568=)	rs756473581	0.00004
NM_004525.3(LRP2):c.1703C>T (p.Ser568Leu)	rs141305635	0.00004
NM_004525.3(LRP2):c.7006C>T (p.Arg2336Trp)	rs149849411	0.00004
NM_004525.3(LRP2):c.3494C>T (p.Ser1165Leu)	rs758407766	0.00002
NM_004525.3(LRP2):c.8848G>T (p.Asp2950Tyr)	rs770098442	0.00002
NM_004525.3(LRP2):c.8702A>G (p.His2901Arg)	rs886055083	0.00001
NM_004525.3(LRP2):c.10108A>T (p.Ile3370Phe)
NM_004525.3(LRP2):c.13880C>G (p.Ser4627Trp)
NM_004525.3(LRP2):c.13894A>C (p.Thr4632Pro)
NM_004525.3(LRP2):c.6469G>C (p.Gly2157Arg)	rs769830564
NM_004525.3(LRP2):c.6470-4A>G
NM_004525.3(LRP2):c.6898A>G (p.Ile2300Val)	rs375117974
NM_004525.3(LRP2):c.8686C>A (p.Pro2896Thr)

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