ClinVar Miner

List of variants in gene combination LDB3, LOC110121486 reported as likely benign by Invitae

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
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.415G>A (p.Glu139Lys) rs374613600 0.00006
NM_001368067.1(LDB3):c.369C>T (p.Asn123=) rs751576160 0.00005
NM_001368067.1(LDB3):c.348C>T (p.Ala116=) rs397516557 0.00004
NM_007078.3(LDB3):c.689+3861C>T rs754704023 0.00004
NM_007078.3(LDB3):c.690-4617G>A rs754174632 0.00004
NM_001368067.1(LDB3):c.427C>T (p.Leu143=) rs763783961 0.00003
NM_001368067.1(LDB3):c.432C>T (p.Gly144=) rs558590519 0.00002
NM_001368067.1(LDB3):c.465C>T (p.Asn155=) rs200462775 0.00002
NM_001368067.1(LDB3):c.435C>G (p.Gly145=) rs367612170 0.00001
NM_001368067.1(LDB3):c.453T>C (p.His151=) rs768048953 0.00001
NM_007078.3(LDB3):c.690-4616C>T rs757618215 0.00001
NM_007078.3(LDB3):c.690-4832C>T rs546887989 0.00001
NM_007078.3(LDB3):c.690-4841C>T rs777780639 0.00001
NM_001368067.1(LDB3):c.394C>T (p.Leu132=)
NM_001368067.1(LDB3):c.414C>T (p.Ile138=) rs372423575
NM_001368067.1(LDB3):c.420G>C (p.Val140=)
NM_001368067.1(LDB3):c.426G>A (p.Gly142=) rs760615794
NM_001368067.1(LDB3):c.432C>A (p.Gly144=)
NM_001368067.1(LDB3):c.468G>A (p.Thr156=) rs745413406
NM_001368067.1(LDB3):c.468G>T (p.Thr156=)
NM_001368067.1(LDB3):c.486C>T (p.Ser162=)
NM_001368067.1(LDB3):c.507C>T (p.Ala169=) rs2132397471
NM_001368067.1(LDB3):c.510C>T (p.Ile170=)
NM_007078.3(LDB3):c.689+3870C>T rs1028583921
NM_007078.3(LDB3):c.689+3904A>T rs776327220
NM_007078.3(LDB3):c.689+3916C>A
NM_007078.3(LDB3):c.690-4606C>T
NM_007078.3(LDB3):c.690-4611C>T rs901009545
NM_007078.3(LDB3):c.690-4612C>T rs2132397872
NM_007078.3(LDB3):c.690-4835T>A rs2132396498
NM_007078.3(LDB3):c.690-4842G>T rs113445294
NM_007078.3(LDB3):c.690-4843C>T

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