ClinVar Miner

List of variants in gene LEP studied for overnutrition

Included ClinVar conditions (59):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_000230.3(LEP):c.*2253C>A rs11761556 0.43092
NM_000230.3(LEP):c.*2205G>A rs41457646 0.10795
NM_000230.3(LEP):c.*400G>T rs17151922 0.09344
NM_000230.3(LEP):c.*366A>T rs28954118 0.03579
NM_000230.3(LEP):c.*1243A>G rs6966536 0.02955
NM_000230.3(LEP):c.280G>A (p.Val94Met) rs17151919 0.02565
NM_000230.3(LEP):c.*34G>A rs28954114 0.01449
NM_000230.3(LEP):c.*2224G>A rs28959472 0.00721
NM_000230.3(LEP):c.*2799C>T rs200887574 0.00666
NM_000230.3(LEP):c.*2015C>A rs28959471 0.00615
NM_000230.3(LEP):c.*150G>A rs28954115 0.00537
NM_000230.3(LEP):c.*1010C>A rs138289049 0.00481
NM_000230.3(LEP):c.*33C>T rs62481073 0.00302
NM_000230.3(LEP):c.*204C>T rs113405088 0.00283
NM_000230.3(LEP):c.*2053G>A rs17617757 0.00215
NM_000230.3(LEP):c.*2110G>T rs187235717 0.00197
NM_000230.3(LEP):c.*373G>A rs183801334 0.00169
NM_000230.3(LEP):c.*300C>T rs191600447 0.00143
NM_000230.3(LEP):c.*1014C>G rs151325384 0.00120
NM_000230.3(LEP):c.*360G>A rs200748706 0.00094
NM_000230.3(LEP):c.*2738G>A rs201644572 0.00093
NM_000230.3(LEP):c.*1260A>G rs144195028 0.00087
NM_000230.3(LEP):c.*1640C>T rs201065449 0.00086
NM_000230.3(LEP):c.*1428C>A rs76601079 0.00057
NM_000230.3(LEP):c.*1678C>T rs188857005 0.00048
NM_000230.3(LEP):c.*2503C>T rs200431904 0.00040
NM_000230.3(LEP):c.*1185C>T rs200556203 0.00026
NM_000230.3(LEP):c.*2245C>G rs201052331 0.00021
NM_000230.3(LEP):c.53A>G (p.Tyr18Cys) rs148407750 0.00021
NM_000230.3(LEP):c.*1124G>A rs3750034 0.00019
NM_000230.3(LEP):c.*2800G>A rs1378129983 0.00014
NM_000230.3(LEP):c.*781G>C rs70940808 0.00011
NM_000230.3(LEP):c.21C>T (p.Cys7=) rs201523305 0.00011
NM_000230.3(LEP):c.165G>A (p.Gln55=) rs138908051 0.00010
NM_000230.3(LEP):c.*1318G>C rs200129463 0.00008
NM_000230.3(LEP):c.*1825T>C rs199792491 0.00008
NM_000230.3(LEP):c.*1886T>G rs201604408 0.00006
NM_000230.3(LEP):c.*653A>C rs201341056 0.00006
NM_000230.3(LEP):c.*1549T>C rs201701012 0.00003
NM_000230.3(LEP):c.212C>A (p.Thr71Asn) rs886061973 0.00003
NM_000230.3(LEP):c.143C>T (p.Thr48Met) rs770247453 0.00002
NM_000230.3(LEP):c.*1369G>T rs1482418354 0.00001
NM_000230.3(LEP):c.*1579G>A rs200802392 0.00001
NM_000230.3(LEP):c.*1637A>G rs780861433 0.00001
NM_000230.3(LEP):c.*1738G>A rs201949587 0.00001
NM_000230.3(LEP):c.*1749T>C rs1483827030 0.00001
NM_000230.3(LEP):c.*57C>T rs1795318328 0.00001
NM_000230.3(LEP):c.*69A>G rs886061974 0.00001
NM_000230.3(LEP):c.*992G>T rs886061976 0.00001
NM_000230.3(LEP):c.144+15C>T rs776318015 0.00001
NM_000230.3(LEP):c.*1422A>T rs1795337523
NM_000230.3(LEP):c.*1720A>G rs10954174
NM_000230.3(LEP):c.*2234G>A rs886061977
NM_000230.3(LEP):c.*2263G>A rs1795349651
NM_000230.3(LEP):c.*2267A>C rs886061978
NM_000230.3(LEP):c.*2410G>A rs28959474
NM_000230.3(LEP):c.*2437C>T rs536449594
NM_000230.3(LEP):c.*2527G>T rs886061979
NM_000230.3(LEP):c.*2579G>A rs200738664
NM_000230.3(LEP):c.*2595C>A rs28959475
NM_000230.3(LEP):c.*2595C>T rs28959475
NM_000230.3(LEP):c.*2819_*2822dup rs56247456
NM_000230.3(LEP):c.*2820_*2822dup rs56247456
NM_000230.3(LEP):c.*2822dup rs56247456
NM_000230.3(LEP):c.*422G>C rs886061975
NM_000230.3(LEP):c.*750G>C rs977939827
NM_000230.3(LEP):c.*785A>G rs114834517
NM_000230.3(LEP):c.*962T>G rs1795330798
NM_000230.3(LEP):c.-14T>G rs1795280375
NM_000230.3(LEP):c.175G>A (p.Gly59Ser) rs200575914
NM_000230.3(LEP):c.181G>A (p.Asp61Asn) rs886061972
NM_000230.3(LEP):c.190C>T (p.Pro64Ser)
NM_000230.3(LEP):c.313C>T (p.Arg105Trp) rs104894023
NM_000230.3(LEP):c.398del (p.Gly133fs)
NM_000230.3(LEP):c.436G>T (p.Ala146Ser) rs1795315989
NM_000230.3(LEP):c.461T>C (p.Leu154Pro) rs1554394014

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