List of variants in gene LRP2 reported as likely benign by Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.3452C>T (p.Pro1151Leu)	rs150552608	0.01319
NM_004525.3(LRP2):c.6858T>A (p.Phe2286Leu)	rs140918583	0.00089
NM_004525.3(LRP2):c.8458C>A (p.Arg2820Ser)	rs140586887	0.00041
NM_004525.3(LRP2):c.1555C>T (p.Pro519Ser)	rs147981204	0.00019
NM_004525.3(LRP2):c.3266G>A (p.Arg1089His)	rs143115109	0.00017
NM_004525.3(LRP2):c.8132G>A (p.Arg2711His)	rs190037522	0.00015
NM_004525.3(LRP2):c.11851G>A (p.Asp3951Asn)	rs761977482	0.00009
NM_004525.3(LRP2):c.7514G>A (p.Arg2505His)	rs371708810	0.00009
NM_004525.3(LRP2):c.11072G>A (p.Arg3691His)	rs142884214	0.00004
NM_004525.3(LRP2):c.7006C>T (p.Arg2336Trp)	rs149849411	0.00004
NM_004525.3(LRP2):c.2213G>C (p.Gly738Ala)	rs762447103	0.00003
NM_004525.3(LRP2):c.4689G>A (p.Met1563Ile)	rs548232056	0.00002
NM_004525.3(LRP2):c.7307C>T (p.Thr2436Ile)	rs771962414	0.00002
NM_004525.3(LRP2):c.6011T>C (p.Leu2004Pro)	rs1338933587	0.00001
NM_004525.3(LRP2):c.9496A>G (p.Lys3166Glu)	rs1423836845

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