ClinVar Miner

Variants in gene LRP4 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 24
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HGVS dbSNP gnomAD frequency
NM_002334.4(LRP4):c.941T>C (p.Leu314Ser) rs7926667 0.05542
NM_002334.4(LRP4):c.1695G>A (p.Glu565=) rs61741501 0.05533
NM_002334.4(LRP4):c.813G>A (p.Thr271=) rs879721 0.05245
NM_002334.4(LRP4):c.129C>G (p.Thr43=) rs61742974 0.04439
NM_002334.4(LRP4):c.*261C>A rs77376145 0.03985
NM_002334.4(LRP4):c.1501A>C (p.Asn501His) rs72897663 0.03190
NM_002334.4(LRP4):c.4837+10C>T rs74806847 0.02574
NM_002334.4(LRP4):c.3945G>A (p.Ser1315=) rs61733844 0.02133
NM_002334.4(LRP4):c.5165T>A (p.Leu1722His) rs117936904 0.01806
NM_002334.4(LRP4):c.1117C>T (p.Arg373Trp) rs118009068 0.01710
NM_002334.4(LRP4):c.431-12G>A rs139371503 0.01241
NM_002334.4(LRP4):c.3817C>A (p.Arg1273=) rs61746928 0.00385
NM_002334.4(LRP4):c.1551T>C (p.Ala517=) rs150777198 0.00314
NM_002334.4(LRP4):c.1828C>T (p.Arg610Cys) rs150253578 0.00289
NM_002334.4(LRP4):c.5357T>A (p.Met1786Lys) rs61748876 0.00225
NM_002334.4(LRP4):c.1494C>T (p.Asn498=) rs61749083 0.00221
NM_002334.4(LRP4):c.1191T>C (p.Asn397=) rs73458078 0.00212
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.677-14T>C rs373597511 0.00053
NM_002334.4(LRP4):c.431-8C>T rs150531536 0.00003
NM_002334.4(LRP4):c.1365A>G (p.Pro455=) rs143481229 0.00001

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