ClinVar Miner

List of variants in gene combination LDB3, LOC110121486 studied for not provided

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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_007078.3(LDB3):c.689+3825G>C rs3740345 0.66820
NM_007078.3(LDB3):c.690-5020A>T rs1578895 0.62980
NM_007078.3(LDB3):c.689+4181C>T rs3802662 0.57883
NM_007078.3(LDB3):c.690-5009T>C rs73344172 0.08333
NM_007078.3(LDB3):c.689+5015A>G rs113972163 0.08279
NM_001368067.1(LDB3):c.504T>C (p.Asp168=) rs76615432 0.06909
NM_007078.3(LDB3):c.690-4842G>A rs113445294 0.06823
NM_007078.3(LDB3):c.690-4476C>T rs78200082 0.05200
NM_007078.3(LDB3):c.690-4345G>A rs117280687 0.01754
NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn) rs121908338 0.00584
NM_007078.3(LDB3):c.689+4041G>A rs73344165 0.00573
NM_007078.3(LDB3):c.690-4896C>G rs113616598 0.00485
NM_001368067.1(LDB3):c.546T>C (p.Ser182=) rs71473272 0.00316
NM_007078.3(LDB3):c.690-4621A>G rs370053163 0.00016
NM_001368067.1(LDB3):c.511G>A (p.Ala171Thr) rs373632943 0.00015
NM_001368067.1(LDB3):c.393C>T (p.Ala131=) rs368832031 0.00013
NM_001368067.1(LDB3):c.345C>T (p.Asn115=) rs562263201 0.00009
NM_001368067.1(LDB3):c.433G>A (p.Gly145Ser) rs376489385 0.00009
NM_001368067.1(LDB3):c.415G>A (p.Glu139Lys) rs374613600 0.00006
NM_001368067.1(LDB3):c.346G>A (p.Ala116Thr) rs200458194 0.00005
NM_001368067.1(LDB3):c.370C>A (p.Pro124Thr) rs755513516 0.00005
NM_001368067.1(LDB3):c.333C>G (p.Asn111Lys) rs369470035 0.00004
NM_001368067.1(LDB3):c.348C>T (p.Ala116=) rs397516557 0.00004
NM_007078.3(LDB3):c.689+3861C>T rs754704023 0.00004
NM_001368067.1(LDB3):c.331A>G (p.Asn111Asp) rs376900496 0.00003
NM_001368067.1(LDB3):c.418G>A (p.Val140Met) rs745329859 0.00001
NM_001368067.1(LDB3):c.430G>A (p.Gly144Ser) rs915830221 0.00001
NM_001368067.1(LDB3):c.545G>A (p.Ser182Asn) rs774522659 0.00001
NM_007078.3(LDB3):c.690-4616C>T rs757618215 0.00001
NM_001368067.1(LDB3):c.358G>A (p.Glu120Lys) rs773370724
NM_001368067.1(LDB3):c.439G>A (p.Ala147Thr) rs121908333
NM_001368067.1(LDB3):c.455C>T (p.Ala152Val) rs753193786
NM_001368067.1(LDB3):c.468G>A (p.Thr156=) rs745413406
NM_001368067.1(LDB3):c.494C>T (p.Ala165Val) rs121908334
NM_001368067.1(LDB3):c.523_524delinsAC (p.Gln175Thr) rs794729064
NM_001368067.1(LDB3):c.527C>T (p.Ala176Val)
NM_007078.3(LDB3):c.689+5016_689+5018dup rs3086887
NM_007078.3(LDB3):c.689+5017_689+5018dup rs3086887
NM_007078.3(LDB3):c.689+5018del rs3086887
NM_007078.3(LDB3):c.689+5018dup rs3086887
NM_007078.3(LDB3):c.690-4571A>C rs111941601
NM_007078.3(LDB3):c.690-4621A>T rs370053163
NM_007078.3(LDB3):c.690-4837C>T rs528725791

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