ClinVar Miner

List of variants in gene SGCD reported as benign

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Gene type:
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Total variants: 44
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HGVS dbSNP
NM_000337.5(SGCD):c.*1527C>T rs284445
NM_000337.5(SGCD):c.*1618T>C rs1389818
NM_000337.5(SGCD):c.*2A>C rs200757725
NM_000337.5(SGCD):c.*3772dup rs397841758
NM_000337.5(SGCD):c.*4395A>T rs10041876
NM_000337.5(SGCD):c.*4813T>C rs1845479
NM_000337.5(SGCD):c.*5863C>T rs11953631
NM_000337.5(SGCD):c.*6717G>A rs1827368
NM_000337.5(SGCD):c.*781G>C rs3857412
NM_000337.5(SGCD):c.-179A>G rs77808502
NM_000337.5(SGCD):c.-303A>T rs7725121
NM_000337.5(SGCD):c.-372C>G rs7717393
NM_000337.5(SGCD):c.-412A>T rs7724969
NM_000337.5(SGCD):c.-43-130G>A
NM_000337.5(SGCD):c.-43-245A>G
NM_000337.5(SGCD):c.-626_-616del rs149976574
NM_000337.5(SGCD):c.-94C>G rs13170573
NM_000337.5(SGCD):c.105G>C (p.Leu35=) rs193922392
NM_000337.5(SGCD):c.144G>C (p.Val48=) rs372152495
NM_000337.5(SGCD):c.15G>C (p.Glu5Asp) rs549319429
NM_000337.5(SGCD):c.192+192G>A
NM_000337.5(SGCD):c.192+86A>G
NM_000337.5(SGCD):c.290G>A (p.Arg97Gln) rs45559835
NM_000337.5(SGCD):c.294+279C>A
NM_000337.5(SGCD):c.294+8T>C rs11748588
NM_000337.5(SGCD):c.295-286G>A
NM_000337.5(SGCD):c.295-40T>A rs74571343
NM_000337.5(SGCD):c.3+19C>T rs182715924
NM_000337.5(SGCD):c.3+20G>A rs187786098
NM_000337.5(SGCD):c.3+248C>T
NM_000337.5(SGCD):c.382+232T>A
NM_000337.5(SGCD):c.383-171A>G
NM_000337.5(SGCD):c.4-143A>G
NM_000337.5(SGCD):c.402T>C (p.Ala134=) rs190935424
NM_000337.5(SGCD):c.503-224T>G
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.575+167A>C
NM_000337.5(SGCD):c.699+18C>G rs180898690
NM_000337.5(SGCD):c.699+71G>A rs187204080
NM_000337.5(SGCD):c.700-19T>C rs80086857
NM_000337.5(SGCD):c.84T>C (p.Tyr28=) rs1801193
NM_000337.5(SGCD):c.91C>G (p.Arg31Gly) rs202223676
NM_001128209.2(SGCD):c.696+13_696+15del rs397517924

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