List of variants in gene LRP4 reported as likely pathogenic

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_002334.4(LRP4):c.1184-1G>A	rs1941502709	0.00001
NM_002334.4(LRP4):c.1633C>T (p.Arg545Trp)	rs371763360	0.00001
NM_002334.4(LRP4):c.1184-2A>G
NM_002334.4(LRP4):c.1560G>A (p.Trp520Ter)	rs1479002757
NM_002334.4(LRP4):c.1894C>T (p.Arg632Cys)	rs1941393359
NM_002334.4(LRP4):c.2507-1G>A
NM_002334.4(LRP4):c.2814+1G>A
NM_002334.4(LRP4):c.3472C>T (p.Arg1158Trp)	rs886048351
NM_002334.4(LRP4):c.3557G>C (p.Trp1186Ser)	rs387906883
NM_002334.4(LRP4):c.3698A>C (p.Glu1233Ala)	rs1940998166
NM_002334.4(LRP4):c.3699+1G>A
NM_002334.4(LRP4):c.409G>A (p.Asp137Asn)	rs267607222
NM_002334.4(LRP4):c.4207G>C (p.Asp1403His)	rs1940965143
NM_002334.4(LRP4):c.4225_4226insC (p.Ile1409fs)
NM_002334.4(LRP4):c.4230-2A>T
NM_002334.4(LRP4):c.4690C>A (p.Gln1564Lys)	rs1940862694
NM_002334.4(LRP4):c.547+1G>A	rs762425885
NM_002334.4(LRP4):c.898G>A (p.Asp300Asn)

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