ClinVar Miner

List of variants in gene LDB3 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 99
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HGVS dbSNP gnomAD frequency
NM_001368063.1(LDB3):c.-23-390A>G rs34073498 0.03113
NM_007078.3(LDB3):c.1978+198A>G rs117918530 0.02468
NM_007078.3(LDB3):c.1676+245A>C rs116015322 0.01286
NM_007078.3(LDB3):c.897-298A>C rs117230487 0.01089
NM_007078.3(LDB3):c.896+6959C>T rs139415121 0.00968
NM_007078.3(LDB3):c.322-305G>A rs11596380 0.00913
NM_007078.3(LDB3):c.2094+162G>A rs112207292 0.00857
NM_007078.3(LDB3):c.689+323T>C rs145371401 0.00726
NM_007078.3(LDB3):c.897-6907A>G rs79068721 0.00651
NM_007078.3(LDB3):c.859+179G>A rs77359721 0.00648
NM_007078.3(LDB3):c.1979-310G>A rs114139889 0.00611
NM_007078.3(LDB3):c.897-164C>A rs11815273 0.00609
NM_007078.3(LDB3):c.1231+209G>A rs143431229 0.00530
NM_007078.3(LDB3):c.1232-97_1232-96insG rs537326671 0.00527
NM_007078.3(LDB3):c.1676+267C>T rs184741262 0.00526
NM_007078.3(LDB3):c.1857+32_1857+33del rs149127817 0.00225
NM_007078.3(LDB3):c.295C>T (p.Pro99Ser) rs201693259 0.00088
NM_007078.3(LDB3):c.466G>A (p.Ala156Thr) rs200596619 0.00082
NM_007078.3(LDB3):c.1036G>A (p.Ala346Thr) rs201968775 0.00054
NM_007078.3(LDB3):c.1111G>A (p.Ala371Thr) rs45539535 0.00054
NM_007078.3(LDB3):c.1045T>A (p.Ser349Thr) rs147042608 0.00051
NM_007078.3(LDB3):c.1312A>G (p.Thr438Ala) rs111941389 0.00048
NM_007078.3(LDB3):c.1594G>C (p.Ala532Pro) rs143764931 0.00036
NM_007078.3(LDB3):c.664G>A (p.Ala222Thr) rs139922045 0.00036
NM_007078.3(LDB3):c.732C>T (p.Pro244=) rs144509718 0.00034
NM_007078.3(LDB3):c.2092G>A (p.Ala698Thr) rs45577134 0.00026
NM_007078.3(LDB3):c.1971C>T (p.Cys657=) rs140552419 0.00025
NM_007078.3(LDB3):c.1606G>A (p.Val536Ile) rs113817827 0.00024
NM_007078.3(LDB3):c.1911G>A (p.Ala637=) rs150710377 0.00020
NM_007078.3(LDB3):c.1910C>T (p.Ala637Val) rs141569007 0.00018
NM_007078.3(LDB3):c.1858-10T>C rs202208256 0.00017
NM_007078.3(LDB3):c.492G>T (p.Pro164=) rs368407147 0.00015
NM_007078.3(LDB3):c.897-14T>C rs763081924 0.00014
NM_007078.3(LDB3):c.342C>T (p.Asn114=) rs151166414 0.00013
NM_007078.3(LDB3):c.714C>T (p.Ala238=) rs727503125 0.00013
NM_007078.3(LDB3):c.794G>A (p.Arg265His) rs45458895 0.00011
NM_007078.3(LDB3):c.897-16G>C rs45513100 0.00011
NM_007078.3(LDB3):c.1071T>A (p.Pro357=) rs143823978 0.00009
NM_007078.3(LDB3):c.493C>T (p.Arg165Trp) rs45610637 0.00009
NM_007078.3(LDB3):c.1075G>A (p.Asp359Asn) rs557956141 0.00008
NM_007078.3(LDB3):c.715G>A (p.Val239Ile) rs201417512 0.00008
NM_007078.3(LDB3):c.-24+18G>A rs1054080127 0.00007
NM_007078.3(LDB3):c.1521C>T (p.Thr507=) rs200838004 0.00006
NM_007078.3(LDB3):c.543C>T (p.Leu181=) rs148324530 0.00006
NM_007078.3(LDB3):c.689+9C>T rs727503124 0.00006
NM_007078.3(LDB3):c.1728C>T (p.Thr576=) rs749988944 0.00005
NM_007078.3(LDB3):c.992C>T (p.Ala331Val) rs368053281 0.00005
NM_007078.3(LDB3):c.1225C>A (p.Gln409Lys) rs139104492 0.00004
NM_007078.3(LDB3):c.1403A>G (p.Asn468Ser) rs730880129 0.00004
NM_007078.3(LDB3):c.407C>T (p.Pro136Leu) rs772887402 0.00004
NM_007078.3(LDB3):c.93+12C>T rs746751581 0.00004
NM_007078.3(LDB3):c.378G>A (p.Ala126=) rs149872184 0.00003
NM_007078.3(LDB3):c.398C>T (p.Pro133Leu) rs200239096 0.00003
NM_007078.3(LDB3):c.567G>A (p.Ser189=) rs778777214 0.00003
NM_007078.3(LDB3):c.897-10G>A rs77304928 0.00003
NM_007078.3(LDB3):c.900C>A (p.Thr300=) rs760071118 0.00003
NM_007078.3(LDB3):c.1164C>T (p.Pro388=) rs780108812 0.00002
NM_007078.3(LDB3):c.1256C>A (p.Ser419Tyr) rs368888118 0.00002
NM_007078.3(LDB3):c.1824G>A (p.Pro608=) rs748428531 0.00002
NM_007078.3(LDB3):c.2124G>A (p.Pro708=) rs759812655 0.00002
NM_007078.3(LDB3):c.468C>T (p.Ala156=) rs374233873 0.00002
NM_007078.3(LDB3):c.646A>T (p.Met216Leu) rs765199175 0.00002
NM_007078.3(LDB3):c.1105A>G (p.Ser369Gly) rs181700296 0.00001
NM_007078.3(LDB3):c.11G>A (p.Ser4Asn) rs766405051 0.00001
NM_007078.3(LDB3):c.1200T>G (p.Thr400=) rs1447980981 0.00001
NM_007078.3(LDB3):c.1437G>C (p.Gly479=) rs960379328 0.00001
NM_007078.3(LDB3):c.1562A>G (p.Tyr521Cys) rs535737552 0.00001
NM_007078.3(LDB3):c.1668T>C (p.Asn556=) rs916700413 0.00001
NM_007078.3(LDB3):c.1677-19C>T rs749512075 0.00001
NM_007078.3(LDB3):c.2091C>T (p.Cys697=) rs571356142 0.00001
NM_007078.3(LDB3):c.2094+10T>C rs769802374 0.00001
NM_007078.3(LDB3):c.246-4A>G rs370264195 0.00001
NM_007078.3(LDB3):c.328G>A (p.Ala110Thr) rs768737496 0.00001
NM_007078.3(LDB3):c.385A>G (p.Ser129Gly) rs794729057 0.00001
NM_007078.3(LDB3):c.540A>G (p.Leu180=) rs1283051092 0.00001
NM_007078.3(LDB3):c.81C>G (p.Leu27=) rs1554844351 0.00001
NM_007078.3(LDB3):c.*13G>T rs397517207
NM_007078.3(LDB3):c.-48G>T rs2803556
NM_007078.3(LDB3):c.1041C>T (p.Ser347=) rs45555240
NM_007078.3(LDB3):c.1167C>T (p.Ala389=) rs768844187
NM_007078.3(LDB3):c.1232-12dup rs752301693
NM_007078.3(LDB3):c.1232-96A>G rs59439194
NM_007078.3(LDB3):c.1296C>T (p.Ser432=) rs753546855
NM_007078.3(LDB3):c.1296CCCTGCCCCTGCCTACACCCCCTC[1] (p.434APAYTPSP[1]) rs397517209
NM_007078.3(LDB3):c.1296CCCTGCCCCTGCCTACACCCCCTC[3] (p.434APAYTPSP[3]) rs397517209
NM_007078.3(LDB3):c.1445C>T (p.Ala482Val) rs774313535
NM_007078.3(LDB3):c.144C>T (p.Leu48=) rs397517213
NM_007078.3(LDB3):c.1752G>C (p.Leu584=) rs1589676711
NM_007078.3(LDB3):c.1815C>T (p.Phe605=) rs1057522289
NM_007078.3(LDB3):c.1858-7C>G rs1057520727
NM_007078.3(LDB3):c.2094+148G>A rs17106978
NM_007078.3(LDB3):c.287T>C (p.Val96Ala) rs794729056
NM_007078.3(LDB3):c.322-100G>A rs150030975
NM_007078.3(LDB3):c.690-17CT[3] rs544039308
NM_007078.3(LDB3):c.860-15C>T rs727503126
NM_007078.3(LDB3):c.897-11C>T rs766463668
NM_007078.3(LDB3):c.93+10C>A rs1222755412
NM_007078.3(LDB3):c.93+272_93+273insGAGG rs141315074
NM_007078.3(LDB3):c.94-119G>C rs4468255

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