ClinVar Miner

List of variants in gene LDB3 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 126
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.1051A>G (p.Thr351Ala) rs138251566 0.00026
NM_007078.3(LDB3):c.1049C>T (p.Thr350Ile) rs200796750 0.00022
NM_007078.3(LDB3):c.769G>C (p.Glu257Gln) rs143996848 0.00016
NM_007078.3(LDB3):c.826C>T (p.Arg276Cys) rs397517226 0.00015
NM_007078.3(LDB3):c.1253C>G (p.Pro418Arg) rs141870580 0.00013
NM_007078.3(LDB3):c.404C>A (p.Thr135Asn) rs1004651681 0.00011
NM_007078.3(LDB3):c.2017G>A (p.Asp673Asn) rs45514002 0.00010
NM_007078.3(LDB3):c.1487T>C (p.Phe496Ser) rs147072071 0.00009
NM_007078.3(LDB3):c.1697T>G (p.Met566Arg) rs566463138 0.00009
NM_007078.3(LDB3):c.1823C>T (p.Pro608Leu) rs145983824 0.00009
NM_007078.3(LDB3):c.1640G>A (p.Arg547Gln) rs201968826 0.00007
NM_007078.3(LDB3):c.1858-11C>A rs369454227 0.00007
NM_007078.3(LDB3):c.533G>A (p.Arg178Gln) rs143311349 0.00006
NM_007078.3(LDB3):c.793C>T (p.Arg265Cys) rs45521338 0.00006
NM_001368067.1(LDB3):c.787C>T (p.Arg263Cys) rs377201153 0.00005
NM_007078.3(LDB3):c.1676G>A (p.Arg559Gln) rs763908636 0.00005
NM_007078.3(LDB3):c.1904T>G (p.Val635Gly) rs567014755 0.00005
NM_007078.3(LDB3):c.2073C>T (p.His691=) rs45486293 0.00005
NM_007078.3(LDB3):c.610G>A (p.Ala204Thr) rs774976112 0.00005
NM_007078.3(LDB3):c.668C>T (p.Ser223Leu) rs375306400 0.00005
NM_007078.3(LDB3):c.1336A>G (p.Thr446Ala) rs1445864873 0.00004
NM_007078.3(LDB3):c.2174T>A (p.Ile725Asn) rs748399477 0.00004
NM_007078.3(LDB3):c.530C>T (p.Ala177Val) rs397517224 0.00004
NM_007078.3(LDB3):c.764A>G (p.Lys255Arg) rs199739130 0.00004
NM_007078.3(LDB3):c.944C>T (p.Pro315Leu) rs371649487 0.00004
NM_001368067.1(LDB3):c.817G>A (p.Gly273Ser) rs771037817 0.00003
NM_007078.3(LDB3):c.1165G>A (p.Ala389Thr) rs924634578 0.00003
NM_007078.3(LDB3):c.1667A>G (p.Asn556Ser) rs372583830 0.00003
NM_007078.3(LDB3):c.2026G>A (p.Val676Met) rs549994359 0.00003
NM_007078.3(LDB3):c.296C>T (p.Pro99Leu) rs148638169 0.00003
NM_007078.3(LDB3):c.428G>A (p.Ser143Asn) rs201773873 0.00003
NM_007078.3(LDB3):c.724G>A (p.Ala242Thr) rs759790522 0.00003
NM_007078.3(LDB3):c.905T>C (p.Ile302Thr) rs777489502 0.00003
NM_007078.3(LDB3):c.1381T>G (p.Tyr461Asp) rs145655904 0.00002
NM_007078.3(LDB3):c.1411C>T (p.Pro471Ser) rs750941511 0.00002
NM_007078.3(LDB3):c.1546C>T (p.Arg516Trp) rs773327911 0.00002
NM_007078.3(LDB3):c.1639C>T (p.Arg547Trp) rs374426474 0.00002
NM_007078.3(LDB3):c.1657C>A (p.His553Asn) rs1488010574 0.00002
NM_007078.3(LDB3):c.1696A>G (p.Met566Val) rs775232208 0.00002
NM_007078.3(LDB3):c.1774G>C (p.Glu592Gln) rs727504944 0.00002
NM_007078.3(LDB3):c.356C>T (p.Ala119Val) rs397517223 0.00002
NM_007078.3(LDB3):c.54G>T (p.Gln18His) rs149348427 0.00002
NM_007078.3(LDB3):c.656G>A (p.Arg219Gln) rs530979771 0.00002
NM_007078.3(LDB3):c.762C>A (p.Asn254Lys) rs1845784706 0.00002
NM_007078.3(LDB3):c.-24+5G>C rs759847996 0.00001
NM_007078.3(LDB3):c.1129G>A (p.Ala377Thr) rs794729061 0.00001
NM_007078.3(LDB3):c.1132C>T (p.Pro378Ser) rs373546361 0.00001
NM_007078.3(LDB3):c.1160G>T (p.Gly387Val) rs753535906 0.00001
NM_007078.3(LDB3):c.1168G>A (p.Ala390Thr) rs748672176 0.00001
NM_007078.3(LDB3):c.1211G>A (p.Arg404Gln) rs150868546 0.00001
NM_007078.3(LDB3):c.1274G>A (p.Ser425Asn) rs370073528 0.00001
NM_007078.3(LDB3):c.139G>A (p.Asp47Asn) rs397517212 0.00001
NM_007078.3(LDB3):c.13G>A (p.Val5Met) rs773170985 0.00001
NM_007078.3(LDB3):c.1502C>T (p.Ala501Val) rs755362259 0.00001
NM_007078.3(LDB3):c.1567C>G (p.Pro523Ala) rs794729062 0.00001
NM_007078.3(LDB3):c.1633A>G (p.Ser545Gly) rs1370639524 0.00001
NM_007078.3(LDB3):c.1772A>G (p.Glu591Gly) rs1358579814 0.00001
NM_007078.3(LDB3):c.1799G>A (p.Arg600Gln) rs747523570 0.00001
NM_007078.3(LDB3):c.200A>G (p.Asn67Ser) rs727504500 0.00001
NM_007078.3(LDB3):c.2060G>A (p.Gly687Asp) rs1230240655 0.00001
NM_007078.3(LDB3):c.2119C>T (p.Gln707Ter) rs771316707 0.00001
NM_007078.3(LDB3):c.2156A>C (p.Lys719Thr) rs544854881 0.00001
NM_007078.3(LDB3):c.253C>T (p.Arg85Cys) rs780200228 0.00001
NM_007078.3(LDB3):c.254G>A (p.Arg85His) rs200420174 0.00001
NM_007078.3(LDB3):c.272C>T (p.Thr91Met) rs769237367 0.00001
NM_007078.3(LDB3):c.443G>A (p.Arg148Gln) rs751254270 0.00001
NM_007078.3(LDB3):c.536A>G (p.Asp179Gly) rs794729058 0.00001
NM_007078.3(LDB3):c.550A>G (p.Lys184Glu) rs774886148 0.00001
NM_007078.3(LDB3):c.56G>C (p.Gly19Ala) rs753314972 0.00001
NM_007078.3(LDB3):c.575C>T (p.Pro192Leu) rs758182278 0.00001
NM_007078.3(LDB3):c.655C>T (p.Arg219Ter) rs727503123 0.00001
NM_007078.3(LDB3):c.80T>C (p.Leu27Pro) rs1057517864 0.00001
NM_007078.3(LDB3):c.845C>T (p.Thr282Met) rs199811186 0.00001
NM_007078.3(LDB3):c.890G>A (p.Arg297Lys) rs1266510625 0.00001
NM_007078.3(LDB3):c.897-11C>G rs766463668 0.00001
NM_007078.3(LDB3):c.913G>C (p.Ala305Pro) rs573547650 0.00001
NM_007078.3(LDB3):c.91C>T (p.Arg31Trp) rs367792378 0.00001
NM_007078.3(LDB3):c.955G>A (p.Ala319Thr) rs151219713 0.00001
NM_007078.3(LDB3):c.991G>A (p.Ala331Thr) rs749520121 0.00001
NM_001368067.1(LDB3):c.772G>A (p.Glu258Lys) rs868365512
NM_001368067.1(LDB3):c.781_783delinsTT (p.Ser261fs)
NM_001368067.1(LDB3):c.785C>T (p.Pro262Leu)
NM_007078.3(LDB3):c.1109C>T (p.Pro370Leu) rs794729060
NM_007078.3(LDB3):c.1157dup (p.Ala389fs) rs2132466099
NM_007078.3(LDB3):c.1166_1167inv (p.Ala389Gly)
NM_007078.3(LDB3):c.1253C>T (p.Pro418Leu) rs141870580
NM_007078.3(LDB3):c.1287C>A (p.Tyr429Ter) rs749776448
NM_007078.3(LDB3):c.1289C>T (p.Thr430Ile) rs746183666
NM_007078.3(LDB3):c.1315C>G (p.Pro439Ala)
NM_007078.3(LDB3):c.1325C>T (p.Ala442Val) rs786205349
NM_007078.3(LDB3):c.133C>T (p.Gln45Ter) rs1057524744
NM_007078.3(LDB3):c.1399C>A (p.Pro467Thr)
NM_007078.3(LDB3):c.1407_1408dup (p.Asn470fs) rs1846880706
NM_007078.3(LDB3):c.1573G>C (p.Gly525Arg) rs794729063
NM_007078.3(LDB3):c.157G>A (p.Asp53Asn) rs2132360328
NM_007078.3(LDB3):c.1601_1602dup (p.Thr535fs) rs1846890164
NM_007078.3(LDB3):c.1609del (p.Gln537fs) rs727503129
NM_007078.3(LDB3):c.1645C>T (p.Pro549Ser) rs1238404909
NM_007078.3(LDB3):c.167A>G (p.Asn56Ser) rs751482077
NM_007078.3(LDB3):c.1748C>T (p.Ser583Phe) rs1263835922
NM_007078.3(LDB3):c.1779G>C (p.Gln593His) rs1291914478
NM_007078.3(LDB3):c.1789T>C (p.Tyr597His) rs727503131
NM_007078.3(LDB3):c.1815C>A (p.Phe605Leu) rs1057522289
NM_007078.3(LDB3):c.1824G>T (p.Pro608=) rs748428531
NM_007078.3(LDB3):c.184C>T (p.His62Tyr) rs779234633
NM_007078.3(LDB3):c.1938C>G (p.Ser646Arg) rs755094215
NM_007078.3(LDB3):c.1978+2_1978+5del rs1554864768
NM_007078.3(LDB3):c.2027del (p.Val676fs) rs2132503498
NM_007078.3(LDB3):c.2030A>C (p.Glu677Ala)
NM_007078.3(LDB3):c.2092G>T (p.Ala698Ser) rs45577134
NM_007078.3(LDB3):c.2094+1G>A rs2132503675
NM_007078.3(LDB3):c.2095-1G>A
NM_007078.3(LDB3):c.212C>G (p.Ser71Cys) rs772249948
NM_007078.3(LDB3):c.2155A>C (p.Lys719Gln) rs397517220
NM_007078.3(LDB3):c.280C>T (p.Pro94Ser) rs565557622
NM_007078.3(LDB3):c.322-1G>A rs794729059
NM_007078.3(LDB3):c.343G>C (p.Gly115Arg) rs397517222
NM_007078.3(LDB3):c.411G>T (p.Glu137Asp)
NM_007078.3(LDB3):c.520C>T (p.Pro174Ser) rs749215979
NM_007078.3(LDB3):c.529dup (p.Ala177fs) rs730880345
NM_007078.3(LDB3):c.532C>T (p.Arg178Trp) rs730880128
NM_007078.3(LDB3):c.76C>T (p.Pro26Ser) rs778865072
NM_007078.3(LDB3):c.79C>T (p.Leu27Phe) rs1554844343
NM_007078.3(LDB3):c.805A>C (p.Asn269His) rs1367297073
NM_007078.3(LDB3):c.843G>A (p.Met281Ile)
NM_007078.3(LDB3):c.896+2T>C rs2132418124

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