List of variants in gene LDB3 reported as likely benign for cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.752A>G (p.Lys251Arg)	rs34423165	0.01671
NM_007078.3(LDB3):c.690-4A>G	rs45529531	0.00427
NM_007078.3(LDB3):c.163G>A (p.Val55Ile)	rs3740343	0.00292
NM_007078.3(LDB3):c.1460G>A (p.Arg487His)	rs146265188	0.00189
NM_007078.3(LDB3):c.1422G>A (p.Ser474=)	rs142625982	0.00136
NM_007078.3(LDB3):c.689+10G>A	rs45563234	0.00125
NM_007078.3(LDB3):c.1653C>T (p.Cys551=)	rs45581435	0.00096
NM_007078.3(LDB3):c.993G>A (p.Ala331=)	rs140347820	0.00095
NM_007078.3(LDB3):c.1535A>C (p.Gln512Pro)	rs138951890	0.00080
NM_001368067.1(LDB3):c.780C>T (p.Asn260=)	rs372789789	0.00061
NM_007078.3(LDB3):c.1045T>A (p.Ser349Thr)	rs147042608	0.00051
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.1051A>G (p.Thr351Ala)	rs138251566	0.00026
NM_007078.3(LDB3):c.2092G>A (p.Ala698Thr)	rs45577134	0.00026
NM_007078.3(LDB3):c.1049C>T (p.Thr350Ile)	rs200796750	0.00022
NM_007078.3(LDB3):c.1858-10T>C	rs202208256	0.00017
NM_007078.3(LDB3):c.1071T>A (p.Pro357=)	rs143823978	0.00009
NM_007078.3(LDB3):c.1231+19G>A	rs763969244	0.00006
NM_007078.3(LDB3):c.543C>T (p.Leu181=)	rs148324530	0.00006
NM_007078.3(LDB3):c.1672A>G (p.Ile558Val)	rs372331627	0.00003
NM_007078.3(LDB3):c.1962G>A (p.Glu654=)	rs201063130	0.00003
NM_007078.3(LDB3):c.336C>T (p.Asp112=)	rs776688376	0.00002
NM_007078.3(LDB3):c.1105A>G (p.Ser369Gly)	rs181700296	0.00001
NM_007078.3(LDB3):c.172G>A (p.Asp58Asn)	rs730880127	0.00001
NM_007078.3(LDB3):c.328G>A (p.Ala110Thr)	rs768737496	0.00001
NM_007078.3(LDB3):c.540A>G (p.Leu180=)	rs1283051092	0.00001
NM_001368067.1(LDB3):c.849C>T (p.Ser283=)	rs1846156972
NM_007078.3(LDB3):c.1896C>A (p.Thr632=)	rs1846967797
NM_007078.3(LDB3):c.2130C>T (p.Tyr710=)	rs752415111
NM_007078.3(LDB3):c.465C>T (p.Leu155=)	rs45516997
NM_007078.3(LDB3):c.672T>C (p.Gly224=)	rs2132373056
NM_007078.3(LDB3):c.692G>T (p.Ser231Ile)	rs1845780199
NM_007078.3(LDB3):c.693C>A (p.Ser231Arg)	rs1845780303

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