List of variants in gene LDB3 reported as uncertain significance for Dilated cardiomyopathy 1C

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 46

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.859+47G>C	rs3740346	0.13647
NM_007078.3(LDB3):c.1074C>T (p.Ala358=)	rs45459491	0.02688
NM_007078.3(LDB3):c.897-6700G>A	rs560431536	0.00018
NM_007078.3(LDB3):c.-24+41G>A	rs45578532	0.00011
NM_007078.3(LDB3):c.794G>A (p.Arg265His)	rs45458895	0.00011
NM_007078.3(LDB3):c.1676G>A (p.Arg559Gln)	rs763908636	0.00008
NM_007078.3(LDB3):c.897-6745C>T	rs746256049	0.00006
NM_007078.3(LDB3):c.793C>T (p.Arg265Cys)	rs45521338	0.00005
NM_001368067.1(LDB3):c.802C>T (p.Arg268Cys)	rs121908335	0.00004
NM_007078.3(LDB3):c.2174T>A (p.Ile725Asn)	rs748399477	0.00004
NM_007078.3(LDB3):c.897-6692C>T	rs1286351667	0.00004
NM_007078.3(LDB3):c.897-6664G>A	rs376355443	0.00003
NM_007078.3(LDB3):c.897-6909G>A	rs532856980	0.00003
NM_007078.3(LDB3):c.1696A>G (p.Met566Val)	rs775232208	0.00002
NM_007078.3(LDB3):c.491C>T (p.Pro164Leu)	rs761907380	0.00002
NM_007078.3(LDB3):c.494G>A (p.Arg165Gln)	rs61857115	0.00002
NM_007078.3(LDB3):c.818G>A (p.Arg273His)	rs763481542	0.00002
NM_007078.3(LDB3):c.897-6831C>T	rs886047355	0.00002
NM_007078.3(LDB3):c.1851T>C (p.Ile617=)	rs145402041	0.00001
NM_007078.3(LDB3):c.30C>G (p.Pro10=)	rs766817285	0.00001
NM_007078.3(LDB3):c.550A>G (p.Lys184Glu)	rs774886148	0.00001
NM_007078.3(LDB3):c.655C>T (p.Arg219Ter)	rs727503123	0.00001
NM_007078.3(LDB3):c.723C>T (p.Ser241=)	rs200580597	0.00001
NM_007078.3(LDB3):c.897-6719C>T	rs975012427	0.00001
NM_007078.3(LDB3):c.897-6861G>A	rs1458669091	0.00001
NM_007078.3(LDB3):c.*30C>G	rs1847531002
NM_007078.3(LDB3):c.1041C>A (p.Ser347=)	rs45555240
NM_007078.3(LDB3):c.1167C>T (p.Ala389=)	rs768844187
NM_007078.3(LDB3):c.1213C>A (p.Pro405Thr)	rs1846584122
NM_007078.3(LDB3):c.1231+949C>T
NM_007078.3(LDB3):c.1622G>A (p.Arg541Gln)
NM_007078.3(LDB3):c.1678G>A (p.Gly560Ser)	rs1846936455
NM_007078.3(LDB3):c.1957G>A (p.Gly653Arg)
NM_007078.3(LDB3):c.1978+1184G>A	rs2132490081
NM_007078.3(LDB3):c.608C>G (p.Ser203Trp)
NM_007078.3(LDB3):c.805A>C (p.Asn269His)	rs1367297073
NM_007078.3(LDB3):c.859+81G>A	rs1845795580
NM_007078.3(LDB3):c.896+11G>A	rs1845818201
NM_007078.3(LDB3):c.896+6695T>C	rs1846150336
NM_007078.3(LDB3):c.896+6814G>A	rs1846157787
NM_007078.3(LDB3):c.896+6872G>A	rs1037329839
NM_007078.3(LDB3):c.896+6957G>A	rs886047354
NM_007078.3(LDB3):c.896+86G>A	rs1845822049
NM_007078.3(LDB3):c.897-6525T>C	rs886047356
NM_007078.3(LDB3):c.897-6702C>G	rs1188752285
NM_007078.3(LDB3):c.897-6707G>A	rs537660741

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