ClinVar Miner

List of variants in gene SGCA reported as benign by GeneDx

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_000023.4(SGCA):c.37+66C>T rs9911548 0.99075
NM_000023.4(SGCA):c.983+240A>T rs2696294 0.96110
NM_000023.4(SGCA):c.312+83C>T rs2696297 0.83281
NM_000023.4(SGCA):c.585-222C>T rs2696296 0.61363
NM_000023.4(SGCA):c.37+298G>A rs2412299 0.53793
NM_000023.4(SGCA):c.747+212C>T rs2696295 0.53440
NM_000023.4(SGCA):c.584+229G>A rs16948744 0.40261
NM_000023.4(SGCA):c.385+167A>G rs11868160 0.16228
NM_000023.4(SGCA):c.313-39C>A rs59944537 0.14899
NM_000023.4(SGCA):c.933C>T (p.Val311=) rs1801191 0.08920
NM_000023.4(SGCA):c.37+23G>A rs79410682 0.04614
NM_000023.4(SGCA):c.528C>T (p.Thr176=) rs1801190 0.00912
NM_000023.4(SGCA):c.*10C>G rs60300808 0.00619
NM_000023.4(SGCA):c.1120C>T (p.Arg374Cys) rs35495899 0.00555
NM_000023.4(SGCA):c.-8G>A rs149296410 0.00248
NM_000023.4(SGCA):c.38-198C>G rs12939159
NM_000023.4(SGCA):c.38-337C>A rs73334777
NM_000023.4(SGCA):c.38-337C>T rs73334777
NM_000023.4(SGCA):c.747+161AC[17] rs3138607
NM_000023.4(SGCA):c.747+161AC[18] rs3138607
NM_000023.4(SGCA):c.747+161AC[19] rs3138607
NM_000023.4(SGCA):c.747+161AC[20] rs3138607
NM_000023.4(SGCA):c.747+161AC[21] rs3138607
NM_000023.4(SGCA):c.747+161AC[22] rs3138607
NM_000023.4(SGCA):c.983+246del rs113182656

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