List of variants in gene LRP2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 29

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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.13685T>C (p.Val4562Ala)	rs142245618	0.00201
NM_004525.3(LRP2):c.12725A>G (p.Asp4242Gly)	rs35942532	0.00171
NM_004525.3(LRP2):c.4351G>T (p.Val1451Phe)	rs146289506	0.00164
NM_004525.3(LRP2):c.3110G>A (p.Arg1037Lys)	rs147058423	0.00133
NM_004525.3(LRP2):c.5209C>T (p.Leu1737Phe)	rs149469954	0.00126
NM_004525.3(LRP2):c.2603C>G (p.Thr868Ser)	rs150752263	0.00100
NM_004525.3(LRP2):c.987G>A (p.Ala329=)	rs141751667	0.00084
NM_004525.3(LRP2):c.5107C>T (p.Pro1703Ser)	rs141260047	0.00024
NM_004525.3(LRP2):c.9040C>T (p.Arg3014Trp)	rs142093111	0.00022
NM_004525.3(LRP2):c.7384_7390+8dup	rs587780382	0.00021
NM_004525.3(LRP2):c.8132G>A (p.Arg2711His)	rs190037522	0.00015
NM_004525.3(LRP2):c.8169C>T (p.Asn2723=)	rs200369596	0.00011
NM_004525.3(LRP2):c.12296-4G>A	rs375166826	0.00009
NM_004525.3(LRP2):c.2485C>T (p.Arg829Trp)	rs368619363	0.00004
NM_004525.3(LRP2):c.2618A>G (p.Asn873Ser)	rs587780383	0.00004
NM_004525.3(LRP2):c.3295C>T (p.His1099Tyr)	rs146463817	0.00004
NM_004525.3(LRP2):c.39C>T (p.Leu13=)	rs529649802	0.00002
NM_004525.3(LRP2):c.910G>A (p.Gly304Arg)	rs570052630	0.00002
NM_004525.3(LRP2):c.2738T>C (p.Met913Thr)	rs587780384	0.00001
NM_004525.3(LRP2):c.4855C>A (p.Leu1619Ile)	rs766931921	0.00001
NM_004525.3(LRP2):c.6442C>T (p.Arg2148Trp)	rs774074912	0.00001
NM_004525.3(LRP2):c.7742C>T (p.Thr2581Met)	rs372305097	0.00001
NM_004525.3(LRP2):c.1018C>G (p.His340Asp)	rs777908550
NM_004525.3(LRP2):c.12125G>A (p.Arg4042His)	rs199874294
NM_004525.3(LRP2):c.3973T>C (p.Cys1325Arg)	rs797045683
NM_004525.3(LRP2):c.4766G>A (p.Arg1589His)	rs587780385
NM_004525.3(LRP2):c.7715+3A>T	rs797045684

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