ClinVar Miner

List of variants in gene LPL reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000237.3(LPL):c.*827A>T rs3208305 0.36238
NM_000237.3(LPL):c.*1671T>C rs13702 0.35875
NM_000237.3(LPL):c.*1846C>T rs15285 0.35731
NM_000237.3(LPL):c.*1250A>G rs3200218 0.19694
NM_000237.3(LPL):c.*796A>G rs11570892 0.17851
NM_000237.3(LPL):c.1164C>A (p.Thr388=) rs316 0.15994
NM_000237.3(LPL):c.*1142C>T rs1059507 0.14544
NM_000237.3(LPL):c.*9G>A rs4922115 0.14446
NM_000237.3(LPL):c.*1742T>C rs1059611 0.12946
NM_000237.2(LPL):c.-281T>G rs1800590 0.12919
NM_000237.3(LPL):c.*853C>T rs1803924 0.09151
NM_000237.3(LPL):c.*1224C>A rs3735964 0.09121
NM_000237.3(LPL):c.1421C>G (p.Ser474Ter) rs328 0.08934
NM_000237.3(LPL):c.435G>A (p.Glu145=) rs248 0.05843
NM_000237.3(LPL):c.405G>A (p.Val135=) rs1121923 0.04960
NM_000237.3(LPL):c.*371T>C rs3289 0.04016
NM_000237.3(LPL):c.*1416T>C rs58998793 0.02343
NM_000237.3(LPL):c.*1783A>T rs17091815 0.02107
NM_000237.3(LPL):c.106G>A (p.Asp36Asn) rs1801177 0.01951
NM_000237.3(LPL):c.*1291G>A rs139240067 0.00549
NM_000237.3(LPL):c.*1928T>C rs79756214 0.00516
NM_000237.3(LPL):c.*29G>A rs7818177 0.00511
NM_000237.3(LPL):c.1135A>G (p.Thr379Ala) rs300 0.00353
NM_000237.3(LPL):c.*949G>A rs11570893 0.00168
NM_000237.3(LPL):c.*1848C>A rs3866471
NM_000237.3(LPL):c.678A>G (p.Pro226=) rs558390128

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