List of variants in gene LRP2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.13134C>G (p.Pro4378=)	rs73970129	0.01063
NM_004525.2(LRP2):c.-147G>C	rs114880772	0.01047
NM_004525.3(LRP2):c.*407T>A	rs145253443	0.00691
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.403G>A (p.Asp135Asn)	rs142594441	0.00340
NM_004525.3(LRP2):c.*444G>A	rs114836292	0.00337
NM_004525.3(LRP2):c.6967C>T (p.Leu2323=)	rs149367019	0.00326
NM_004525.3(LRP2):c.-5C>T	rs373286009	0.00255
NM_004525.3(LRP2):c.1973A>G (p.Tyr658Cys)	rs111360923	0.00248
NM_004525.3(LRP2):c.2079C>T (p.Phe693=)	rs145709922	0.00246
NM_004525.3(LRP2):c.*18G>A	rs141693983	0.00226
NM_004525.3(LRP2):c.11663G>A (p.Arg3888His)	rs77686710	0.00218
NM_004525.3(LRP2):c.12379C>A (p.Arg4127Ser)	rs148356370	0.00217
NM_004525.3(LRP2):c.10170-15T>G	rs144579935	0.00205
NM_004525.3(LRP2):c.13685T>C (p.Val4562Ala)	rs142245618	0.00201
NM_004525.3(LRP2):c.12380G>A (p.Arg4127His)	rs142934522	0.00195
NM_004525.3(LRP2):c.2513+14T>C	rs201785482	0.00195
NM_004525.3(LRP2):c.10233C>T (p.Phe3411=)	rs139363553	0.00183
NM_004525.3(LRP2):c.3122A>G (p.Asn1041Ser)	rs143028579	0.00170
NM_004525.3(LRP2):c.4351G>T (p.Val1451Phe)	rs146289506	0.00164
NM_004525.3(LRP2):c.9147C>T (p.Phe3049=)	rs146115458	0.00154
NM_004525.3(LRP2):c.*530C>T	rs115478975	0.00153
NM_004525.3(LRP2):c.12287T>C (p.Ile4096Thr)	rs137922929	0.00129
NM_004525.3(LRP2):c.5209C>T (p.Leu1737Phe)	rs149469954	0.00126
NM_004525.3(LRP2):c.13921A>T (p.Thr4641Ser)	rs79179577	0.00123
NM_004525.3(LRP2):c.170C>T (p.Ala57Val)	rs115350461	0.00111
NM_004525.3(LRP2):c.391A>G (p.Arg131Gly)	rs34592807	0.00109
NM_004525.3(LRP2):c.2603C>G (p.Thr868Ser)	rs150752263	0.00100
NM_004525.3(LRP2):c.6176C>T (p.Ser2059Phe)	rs148299415	0.00098
NM_004525.3(LRP2):c.9617G>A (p.Arg3206His)	rs148251117	0.00073
NM_004525.3(LRP2):c.6256A>T (p.Thr2086Ser)	rs146149181	0.00045
NM_004525.3(LRP2):c.2511C>T (p.Ala837=)	rs375313914	0.00034
NM_004525.3(LRP2):c.*1118T>G	rs575232276	0.00028
NM_004525.3(LRP2):c.*158T>C	rs183814447	0.00028
NM_004525.3(LRP2):c.*297A>G	rs192934188	0.00028
NM_004525.3(LRP2):c.3128A>G (p.Tyr1043Cys)	rs201299366	0.00021
NM_004525.3(LRP2):c.10768+12C>T	rs17848185	0.00020
NM_004525.3(LRP2):c.12296-7T>A	rs200755164	0.00013
NM_004525.3(LRP2):c.13359C>T (p.Ser4453=)	rs202161925	0.00011
NM_004525.3(LRP2):c.*739C>G	rs193064620	0.00009
NM_004525.3(LRP2):c.12296-4G>A	rs375166826	0.00009
NM_004525.3(LRP2):c.8228C>T (p.Pro2743Leu)	rs545645633	0.00005
NM_004525.3(LRP2):c.11244C>T (p.Asn3748=)	rs542010522	0.00001
NM_004525.3(LRP2):c.9342C>T (p.Cys3114=)	rs199803029	0.00001
NM_004525.3(LRP2):c.*1381GATG[6]	rs3083261
NM_004525.3(LRP2):c.11498-13del	rs143342962
NM_004525.3(LRP2):c.12125G>A (p.Arg4042His)	rs199874294
NM_004525.3(LRP2):c.8699-8C>T	rs145301652

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