ClinVar Miner

List of variants in gene SGCD reported as likely benign for Dilated Cardiomyopathy, Dominant

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Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
NM_000337.5(SGCD):c.*1112G>A rs566338494
NM_000337.5(SGCD):c.*1373A>G rs72803041
NM_000337.5(SGCD):c.*150G>T rs147791150
NM_000337.5(SGCD):c.*1846_*1847dupTT rs527436848
NM_000337.5(SGCD):c.*2236T>C rs183838407
NM_000337.5(SGCD):c.*2365T>C rs72803042
NM_000337.5(SGCD):c.*2697T>C rs146249602
NM_000337.5(SGCD):c.*2712T>C rs56293630
NM_000337.5(SGCD):c.*2814G>T rs142023087
NM_000337.5(SGCD):c.*3292A>G rs148505840
NM_000337.5(SGCD):c.*3413G>C rs72803043
NM_000337.5(SGCD):c.*360A>G rs72803040
NM_000337.5(SGCD):c.*363C>T rs6886827
NM_000337.5(SGCD):c.*3650G>T rs72803044
NM_000337.5(SGCD):c.*3687A>G rs72803046
NM_000337.5(SGCD):c.*3868C>A rs181847929
NM_000337.5(SGCD):c.*3898C>T rs74717343
NM_000337.5(SGCD):c.*3962G>A rs56182215
NM_000337.5(SGCD):c.*4092A>G rs56389540
NM_000337.5(SGCD):c.*4166T>C rs55653598
NM_000337.5(SGCD):c.*4498G>A rs73304958
NM_000337.5(SGCD):c.*4638C>A rs187538595
NM_000337.5(SGCD):c.*4818G>A rs76466586
NM_000337.5(SGCD):c.*4895G>A rs115905727
NM_000337.5(SGCD):c.*5114C>T rs3913482
NM_000337.5(SGCD):c.*5226G>A rs552358256
NM_000337.5(SGCD):c.*5348T>C rs149021597
NM_000337.5(SGCD):c.*5663A>G rs151214419
NM_000337.5(SGCD):c.*5723delA rs147634470
NM_000337.5(SGCD):c.*5877C>A rs117879283
NM_000337.5(SGCD):c.*5990T>A rs72803047
NM_000337.5(SGCD):c.*6400C>T rs10065295
NM_000337.5(SGCD):c.*6430G>A rs185162959
NM_000337.5(SGCD):c.*6665G>A rs61633788
NM_000337.5(SGCD):c.*6683T>C rs73304961
NM_000337.5(SGCD):c.*6917C>T rs549743616
NM_000337.5(SGCD):c.*7300C>A rs72803048
NM_000337.5(SGCD):c.*7596A>G rs80115276
NM_000337.5(SGCD):c.*7814C>T rs56233900
NM_000337.5(SGCD):c.*7816G>A rs78589560
NM_000337.5(SGCD):c.*7866G>A rs115728448
NM_000337.5(SGCD):c.*822C>T rs78615220
NM_000337.5(SGCD):c.-179A>G rs77808502
NM_000337.5(SGCD):c.-303A>T rs7725121
NM_000337.5(SGCD):c.-404G>A rs192662989
NM_000337.5(SGCD):c.15G>C (p.Glu5Asp) rs549319429
NM_000337.5(SGCD):c.213G>A (p.Arg71=) rs74846539
NM_000337.5(SGCD):c.290G>A (p.Arg97Gln) rs45559835
NM_000337.5(SGCD):c.294+8T>C rs11748588
NM_000337.5(SGCD):c.507G>A (p.Ala169=) rs10071079
NM_000337.5(SGCD):c.510G>A (p.Glu170=) rs368838376
NM_000337.5(SGCD):c.848A>G (p.Gln283Arg) rs397516338

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