List of variants in gene LRP2 reported by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_004525.3(LRP2):c.63G>C (p.Ala21=)	rs1559014	0.99771
NM_004525.3(LRP2):c.79+15A>G	rs1559013	0.98894
NM_004525.3(LRP2):c.12280A>G (p.Lys4094Glu)	rs2075252	0.79497
NM_004525.3(LRP2):c.2025C>T (p.Val675=)	rs830994	0.61350
NM_004525.3(LRP2):c.12628A>C (p.Ile4210Leu)	rs4667591	0.60691
NM_004525.3(LRP2):c.13113C>T (p.Ile4371=)	rs990626	0.59977
NM_004525.3(LRP2):c.2460A>G (p.Thr820=)	rs2241190	0.54408
NM_004525.3(LRP2):c.3069A>G (p.Thr1023=)	rs831043	0.53755
NM_004525.3(LRP2):c.3550+14C>T	rs2075254	0.53578
NM_004525.3(LRP2):c.3667+20A>C	rs831041	0.52466
NM_004525.3(LRP2):c.10503G>A (p.Gln3501=)	rs2229265	0.45093
NM_004525.3(LRP2):c.3054C>A (p.Thr1018=)	rs2075249	0.41290
NM_004525.3(LRP2):c.4875T>C (p.Cys1625=)	rs2229267	0.38704
NM_004525.3(LRP2):c.248A>G (p.Asn83Ser)	rs2229263	0.33289
NM_004525.3(LRP2):c.8614G>A (p.Ala2872Thr)	rs2228171	0.25207
NM_004525.3(LRP2):c.11996T>G (p.Val3999Gly)	rs79723119	0.00834
NM_004525.3(LRP2):c.2933C>T (p.Thr978Met)	rs114842875	0.00322
NM_004525.3(LRP2):c.10937G>A (p.Arg3646His)	rs142549310	0.00298
NM_004525.3(LRP2):c.92C>T (p.Ala31Val)	rs144829356	0.00280
NM_004525.3(LRP2):c.12380G>A (p.Arg4127His)	rs142934522	0.00195
NM_004525.3(LRP2):c.9363C>T (p.Gly3121=)	rs146783211	0.00039
NM_004525.3(LRP2):c.2688C>G (p.His896Gln)	rs1306828984	0.00001
NM_004525.3(LRP2):c.8623C>T (p.Arg2875Cys)	rs1308246487	0.00001
NM_004525.3(LRP2):c.3550+18T>G	rs2075255
NM_004525.3(LRP2):c.8699-8C>T	rs145301652

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