Variants in gene LRP2 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.923-6G>A	rs144147038	0.00611
NM_004525.3(LRP2):c.8892G>A (p.Arg2964=)	rs149148763	0.00557
NM_004525.3(LRP2):c.149C>G (p.Thr50Ser)	rs114460450	0.00342
NM_004525.3(LRP2):c.10937G>A (p.Arg3646His)	rs142549310	0.00298
NM_004525.3(LRP2):c.1973A>G (p.Tyr658Cys)	rs111360923	0.00248
NM_004525.3(LRP2):c.5390A>G (p.Asn1797Ser)	rs138070797	0.00234
NM_004525.3(LRP2):c.13685T>C (p.Val4562Ala)	rs142245618	0.00201
NM_004525.3(LRP2):c.12725A>G (p.Asp4242Gly)	rs35942532	0.00171
NM_004525.3(LRP2):c.5209C>T (p.Leu1737Phe)	rs149469954	0.00126
NM_004525.3(LRP2):c.1176C>T (p.Gly392=)	rs369145798	0.00070
NM_004525.3(LRP2):c.10165A>G (p.Ile3389Val)	rs140272085	0.00055
NM_004525.3(LRP2):c.12296-4G>A	rs375166826	0.00009
NM_004525.3(LRP2):c.39C>T (p.Leu13=)	rs529649802	0.00002
NM_004525.3(LRP2):c.12125G>A (p.Arg4042His)	rs199874294
NM_004525.3(LRP2):c.428-8del	rs370823033

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