List of variants in gene LRP2 reported as likely benign by Ambry Genetics

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.2456G>A (p.Arg819His)	rs142080405	0.00306
NM_004525.3(LRP2):c.10937G>A (p.Arg3646His)	rs142549310	0.00298
NM_004525.3(LRP2):c.9477G>A (p.Met3159Ile)	rs144322413	0.00152
NM_004525.3(LRP2):c.13921A>T (p.Thr4641Ser)	rs79179577	0.00123
NM_004525.3(LRP2):c.6858T>A (p.Phe2286Leu)	rs140918583	0.00089
NM_004525.3(LRP2):c.9311G>A (p.Ser3104Asn)	rs139523655	0.00089
NM_004525.3(LRP2):c.3311A>G (p.His1104Arg)	rs144906000	0.00073
NM_004525.3(LRP2):c.7747G>A (p.Val2583Met)	rs145201961	0.00063
NM_004525.3(LRP2):c.10165A>G (p.Ile3389Val)	rs140272085	0.00055
NM_004525.3(LRP2):c.7866C>T (p.Asp2622=)	rs139514301	0.00047
NM_004525.3(LRP2):c.7007G>A (p.Arg2336Gln)	rs147287428	0.00045
NM_004525.3(LRP2):c.12421G>A (p.Val4141Ile)	rs150382715	0.00041
NM_004525.3(LRP2):c.5107C>T (p.Pro1703Ser)	rs141260047	0.00024
NM_004525.3(LRP2):c.3355C>A (p.His1119Asn)	rs183570870	0.00021
NM_004525.3(LRP2):c.6130G>A (p.Ala2044Thr)	rs142266106	0.00021
NM_004525.3(LRP2):c.12958A>G (p.Ile4320Val)	rs141452561	0.00019
NM_004525.3(LRP2):c.12923C>T (p.Thr4308Met)	rs543890594	0.00014
NM_004525.3(LRP2):c.2113A>G (p.Ile705Val)	rs140552043	0.00005
NM_004525.3(LRP2):c.593G>A (p.Arg198His)	rs372596334	0.00005
NM_004525.3(LRP2):c.10757G>A (p.Arg3586His)	rs762352363	0.00004
NM_004525.3(LRP2):c.2464G>A (p.Val822Ile)	rs1222200565	0.00001
NM_004525.3(LRP2):c.9257G>A (p.Arg3086His)	rs141866144	0.00001
NM_004525.3(LRP2):c.986C>T (p.Ala329Val)	rs568958746	0.00001
NM_004525.3(LRP2):c.1186A>G (p.Ile396Val)	rs527397264
NM_004525.3(LRP2):c.13832C>T (p.Ala4611Val)
NM_004525.3(LRP2):c.6001G>A (p.Val2001Ile)
NM_004525.3(LRP2):c.6470-4A>G

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