List of variants in gene LRP4 reported as likely benign by Fulgent Genetics, Fulgent 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: 36

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HGVS	dbSNP	gnomAD frequency
NM_002334.4(LRP4):c.431-12G>A	rs139371503	0.01289
NM_002334.4(LRP4):c.430+15C>T	rs199835230	0.00108
NM_002334.4(LRP4):c.4951+13G>C	rs367744491	0.00079
NM_002334.4(LRP4):c.1005C>T (p.Asn335=)	rs141757569	0.00077
NM_002334.4(LRP4):c.387C>T (p.Cys129=)	rs80333596	0.00076
NM_002334.4(LRP4):c.3390G>A (p.Ala1130=)	rs144639401	0.00060
NM_002334.4(LRP4):c.677-14T>C	rs373597511	0.00059
NM_002334.4(LRP4):c.273C>T (p.Asp91=)	rs150401820	0.00025
NM_002334.4(LRP4):c.3384G>A (p.Gly1128=)	rs144335505	0.00021
NM_002334.4(LRP4):c.4584-4G>A	rs368518969	0.00014
NM_002334.4(LRP4):c.2436T>C (p.Asp812=)	rs201159730	0.00012
NM_002334.4(LRP4):c.447C>T (p.Ser149=)	rs763246909	0.00012
NM_002334.4(LRP4):c.3267C>T (p.Asp1089=)	rs150616375	0.00010
NM_002334.4(LRP4):c.4110C>T (p.Asp1370=)	rs143496445	0.00010
NM_002334.4(LRP4):c.1707C>T (p.Tyr569=)	rs61748895	0.00009
NM_002334.4(LRP4):c.2216-14C>T	rs369714698	0.00009
NM_002334.4(LRP4):c.426G>A (p.Gln142=)	rs371955690	0.00009
NM_002334.4(LRP4):c.1048+20G>A	rs199512829	0.00006
NM_002334.4(LRP4):c.177C>T (p.Asp59=)	rs373625784	0.00006
NM_002334.4(LRP4):c.4812C>T (p.Ile1604=)	rs753496184	0.00006
NM_002334.4(LRP4):c.3585C>T (p.Ser1195=)	rs148361325	0.00005
NM_002334.4(LRP4):c.4584-15T>C	rs777314555	0.00005
NM_002334.4(LRP4):c.5556C>T (p.Ala1852=)	rs200514161	0.00005
NM_002334.4(LRP4):c.5088-20C>T	rs370004451	0.00004
NM_002334.4(LRP4):c.431-8C>T	rs150531536	0.00003
NM_002334.4(LRP4):c.3939C>T (p.Cys1313=)	rs779892727	0.00002
NM_002334.4(LRP4):c.1049-6G>C	rs775792196	0.00001
NM_002334.4(LRP4):c.1310-7T>A	rs1555174059	0.00001
NM_002334.4(LRP4):c.1365A>G (p.Pro455=)	rs143481229	0.00001
NM_002334.4(LRP4):c.1815C>T (p.Ile605=)	rs776484339	0.00001
NM_002334.4(LRP4):c.2424+13G>A	rs374365893	0.00001
NM_002334.4(LRP4):c.3195C>T (p.Asp1065=)	rs745991521	0.00001
NM_002334.4(LRP4):c.339C>T (p.Asp113=)	rs368971854	0.00001
NM_002334.4(LRP4):c.200-26TTTTC[2]	rs760673637
NM_002334.4(LRP4):c.3004+18C>T	rs2306028
NM_002334.4(LRP4):c.3278-8C>T	rs1941033938

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