List of variants in gene LRP4 reported as likely benign by GeneDx

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_002334.4(LRP4):c.431-12G>A	rs139371503	0.01289
NM_002334.4(LRP4):c.2506+139G>A	rs112838289	0.01219
NM_002334.4(LRP4):c.4837+112A>C	rs112479534	0.01199
NM_002334.4(LRP4):c.3277+140T>C	rs112168929	0.01198
NM_002334.4(LRP4):c.4230-109C>T	rs141085397	0.01159
NM_002334.4(LRP4):c.4229+57G>A	rs114911553	0.00930
NM_002334.4(LRP4):c.*54G>A	rs147627264	0.00852
NM_002334.4(LRP4):c.3278-152C>G	rs3816615	0.00824
NM_002334.4(LRP4):c.922+225G>C	rs74702051	0.00791
NM_002334.4(LRP4):c.1184-49G>T	rs189768863	0.00782
NM_002334.4(LRP4):c.2814+30G>A	rs181438771	0.00762
NM_002334.4(LRP4):c.4584-36C>T	rs2306030	0.00741
NM_002334.4(LRP4):c.53-110G>A	rs77504414	0.00717
NM_002334.4(LRP4):c.1698-31C>T	rs140605896	0.00692
NM_002334.4(LRP4):c.797-335A>G	rs532482330	0.00663
NM_002334.4(LRP4):c.796+312G>A	rs74933738	0.00654
NM_002334.4(LRP4):c.200-265C>A	rs113354168	0.00550
NM_002334.4(LRP4):c.430+32G>T	rs112786173	0.00549
NM_002334.4(LRP4):c.3537-242C>T	rs78746913	0.00504
NM_002334.4(LRP4):c.2612+206C>T	rs184463185	0.00387
NM_002334.4(LRP4):c.3817C>A (p.Arg1273=)	rs61746928	0.00385
NM_002334.4(LRP4):c.2151C>T (p.Gly717=)	rs114920029	0.00361
NM_002334.4(LRP4):c.1551T>C (p.Ala517=)	rs150777198	0.00307
NM_002334.4(LRP4):c.5357T>A (p.Met1786Lys)	rs61748876	0.00246
NM_002334.4(LRP4):c.1191T>C (p.Asn397=)	rs73458078	0.00233
NM_002334.4(LRP4):c.1494C>T (p.Asn498=)	rs61749083	0.00221
NM_002334.4(LRP4):c.3620A>G (p.Asn1207Ser)	rs151234321	0.00086
NM_002334.4(LRP4):c.636C>T (p.Gly212=)	rs17848239	0.00015
NM_002334.4(LRP4):c.1365A>G (p.Pro455=)	rs143481229	0.00001
NM_002334.4(LRP4):c.1697+133C>G	rs548582739
NM_002334.4(LRP4):c.2814+13_2814+35del
NM_002334.4(LRP4):c.796+66_796+75del	rs201199587

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