ClinVar Miner

List of variants in gene LEP studied for Monogenic Non-Syndromic Obesity

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Gene type:
ClinVar version:
Total variants: 42
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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.*204C>T rs113405088 0.00283
NM_000230.3(LEP):c.*2053G>A rs17617757 0.00215
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.21C>T (p.Cys7=) rs201523305 0.00011
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.*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.*1720A>G rs10954174
NM_000230.3(LEP):c.*2234G>A rs886061977
NM_000230.3(LEP):c.*2267A>C rs886061978
NM_000230.3(LEP):c.*2410G>A rs28959474
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.*785A>G rs114834517
NM_000230.3(LEP):c.181G>A (p.Asp61Asn) rs886061972

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