ClinVar Miner

List of variants in gene LEPR reported as likely benign for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_002303.6(LEPR):c.1029T>C (p.Ser343=) rs1805134 0.23693
NM_002303.6(LEPR):c.2597+15G>C rs6693573 0.01870
NM_002303.6(LEPR):c.1285+20G>A rs13306522 0.01792
NM_002303.6(LEPR):c.370+129G>C rs35971550 0.01633
NM_002303.6(LEPR):c.3024A>G (p.Ser1008=) rs6413506 0.01632
NM_002303.6(LEPR):c.704-26A>G rs112799921 0.01432
NM_002303.6(LEPR):c.2674-3175T>G rs114729793 0.01408
NM_002303.6(LEPR):c.*232G>A rs116819844 0.01407
NM_002303.6(LEPR):c.2598-208C>T rs114989957 0.01405
NM_002303.6(LEPR):c.2673+3114T>A rs78387296 0.01405
NM_002303.6(LEPR):c.371-80C>G rs13306519 0.01285
NM_002303.6(LEPR):c.2673+3223C>T rs115582663 0.01142
NM_002303.6(LEPR):c.850-246C>T rs189230172 0.00660
NM_002303.6(LEPR):c.2958C>T (p.Tyr986=) rs1805095 0.00643
NM_002303.6(LEPR):c.494+324A>T rs116349491 0.00540
NM_002303.6(LEPR):c.36T>C (p.His12=) rs147768538 0.00286
NM_002303.6(LEPR):c.3417A>G (p.Ala1139=) rs61781316 0.00257
NM_002303.6(LEPR):c.371A>G (p.Asp124Gly) rs35573508 0.00192
NM_002303.6(LEPR):c.2260G>A (p.Val754Met) rs150936702 0.00071
NM_002303.6(LEPR):c.3479T>C (p.Met1160Thr) rs145685060 0.00069
NM_002303.6(LEPR):c.3078T>C (p.Asn1026=) rs34130975 0.00054
NM_002303.6(LEPR):c.1246C>T (p.His416Tyr) rs144710810 0.00043
NM_002303.6(LEPR):c.1713G>T (p.Gln571His) rs141393785 0.00031
NM_002303.6(LEPR):c.371-26_371-25insG rs767256351 0.00031
NM_002303.6(LEPR):c.1030G>A (p.Val344Ile) rs145668112 0.00026
NM_002303.6(LEPR):c.3019A>T (p.Ser1007Cys) rs145651189 0.00020
NM_002303.6(LEPR):c.296G>A (p.Cys99Tyr) rs548848340 0.00009
NM_002303.6(LEPR):c.866C>T (p.Ser289Leu) rs760392591 0.00004
NM_002303.6(LEPR):c.2221G>A (p.Val741Met) rs532294036 0.00003
NM_002303.6(LEPR):c.1018A>G (p.Ile340Val) rs753573139 0.00002
NM_002303.6(LEPR):c.371-9T>A rs1253993053 0.00001
NM_002303.6(LEPR):c.921G>C (p.Gln307His) rs531183918 0.00001
NM_002303.6(LEPR):c.1286-11G>A
NM_002303.6(LEPR):c.1298A>G (p.Asn433Ser)
NM_002303.6(LEPR):c.1368A>G (p.Ser456=)
NM_002303.6(LEPR):c.1373C>T (p.Ala458Val)
NM_002303.6(LEPR):c.1481G>A (p.Gly494Asp)
NM_002303.6(LEPR):c.1518A>G (p.Leu506=)
NM_002303.6(LEPR):c.1603+14C>T
NM_002303.6(LEPR):c.1603+15G>C
NM_002303.6(LEPR):c.1623C>G (p.Ser541=)
NM_002303.6(LEPR):c.180G>A (p.Ser60=)
NM_002303.6(LEPR):c.1813G>T (p.Ala605Ser)
NM_002303.6(LEPR):c.1968G>C (p.Lys656Asn) rs1805094
NM_002303.6(LEPR):c.2334T>C (p.Asn778=)
NM_002303.6(LEPR):c.2415G>A (p.Glu805=)
NM_002303.6(LEPR):c.2598-20G>A
NM_002303.6(LEPR):c.2724T>C (p.Cys908=)
NM_002303.6(LEPR):c.2919C>T (p.Thr973=) rs2101047106
NM_002303.6(LEPR):c.2922T>C (p.Tyr974=)
NM_002303.6(LEPR):c.2928C>T (p.Asp976=)
NM_002303.6(LEPR):c.3027C>G (p.Val1009=)
NM_002303.6(LEPR):c.3090G>A (p.Glu1030=)
NM_002303.6(LEPR):c.309A>C (p.Ala103=)
NM_002303.6(LEPR):c.3280T>C (p.Leu1094=)
NM_002303.6(LEPR):c.3285T>G (p.Thr1095=)
NM_002303.6(LEPR):c.3294A>G (p.Ser1098=)
NM_002303.6(LEPR):c.3441T>G (p.Thr1147=)
NM_002303.6(LEPR):c.371-17T>G
NM_002303.6(LEPR):c.40+239_40+240insAC rs67805092
NM_002303.6(LEPR):c.40+239_40+240insACACAC rs67805092
NM_002303.6(LEPR):c.40+240_40+243del rs1440292866
NM_002303.6(LEPR):c.40+241CA[11] rs1009206304
NM_002303.6(LEPR):c.504G>A (p.Val168=)
NM_002303.6(LEPR):c.575A>C (p.Glu192Ala)
NM_002303.6(LEPR):c.695T>G (p.Ile232Arg)
NM_002303.6(LEPR):c.704-17T>C
NM_002303.6(LEPR):c.704-19T>C
NM_002303.6(LEPR):c.81A>G (p.Pro27=)
NM_002303.6(LEPR):c.873A>T (p.Thr291=)
NM_002303.6(LEPR):c.893T>C (p.Ile298Thr)

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