ClinVar Miner

List of variants in gene SGCD reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_000337.6(SGCD):c.192+192G>A rs9313890 0.98637
NM_000337.6(SGCD):c.575+167A>C rs32055 0.91859
NM_000337.6(SGCD):c.*6717G>A rs1827368 0.90216
NM_000337.6(SGCD):c.192+86A>G rs4434364 0.77068
NM_000337.6(SGCD):c.4-143A>G rs8180473 0.57632
NM_000337.6(SGCD):c.-43-245A>G rs11744154 0.41421
NM_000337.6(SGCD):c.-43-130G>A rs11740347 0.41389
NM_000337.6(SGCD):c.84T>C (p.Tyr28=) rs1801193 0.39558
NM_000337.6(SGCD):c.503-224T>G rs39925 0.37569
NM_000337.6(SGCD):c.382+232T>A rs181875 0.32738
NM_000337.6(SGCD):c.294+279C>A rs256826 0.20785
NM_000337.6(SGCD):c.*3772dup rs397841758 0.20069
NM_000337.6(SGCD):c.3+248C>T rs10447212 0.15850
NM_000337.6(SGCD):c.*5863C>T rs11953631 0.15411
NM_000337.6(SGCD):c.295-286G>A rs280475 0.13534
NM_000337.6(SGCD):c.*4092A>G rs56389540 0.09897
NM_000337.6(SGCD):c.*3650G>T rs72803044 0.08674
NM_000337.6(SGCD):c.*3962G>A rs56182215 0.08205
NM_000337.6(SGCD):c.*3687A>G rs72803046 0.08194
NM_000337.6(SGCD):c.700-141C>T rs72803039 0.06886
NM_000337.6(SGCD):c.*7300C>A rs72803048 0.06455
NM_000337.5(SGCD):c.-303A>T rs7725121 0.06375
NM_000337.6(SGCD):c.3+285A>G rs142576328 0.04772
NM_000337.6(SGCD):c.290G>A (p.Arg97Gln) rs45559835 0.04292
NM_000337.6(SGCD):c.294+124A>G rs115859006 0.04023
NM_000337.6(SGCD):c.383-171A>G rs888841 0.02355
NM_000337.6(SGCD):c.*7596A>G rs80115276 0.02244
NM_000337.6(SGCD):c.700-19T>C rs80086857 0.02231
NM_000337.6(SGCD):c.576-84G>T rs115753043 0.02060
NM_000337.6(SGCD):c.295-40T>A rs74571343 0.01950
NM_000337.6(SGCD):c.294+89A>G rs11957790 0.01883
NC_000005.10:g.156326739C>A rs114128937 0.01260
NM_000337.5(SGCD):c.-179A>G rs77808502 0.00918
NM_000337.6(SGCD):c.507G>A (p.Ala169=) rs10071079 0.00680
NM_000337.6(SGCD):c.294+8T>C rs11748588 0.00640
NM_000337.6(SGCD):c.699+71G>A rs187204080 0.00245
NM_000337.6(SGCD):c.*2A>C rs200757725 0.00241
NM_000337.6(SGCD):c.213G>A (p.Arg71=) rs74846539 0.00115
NM_000337.6(SGCD):c.144G>C (p.Val48=) rs372152495 0.00106
NM_000337.5(SGCD):c.-352T>C rs727503419 0.00043
NM_000337.6(SGCD):c.510G>A (p.Glu170=) rs368838376 0.00029
NM_000337.6(SGCD):c.123C>G (p.Leu41=) rs200670993 0.00015
NM_000337.6(SGCD):c.3+20G>A rs187786098 0.00013
NM_000337.6(SGCD):c.402T>C (p.Ala134=) rs190935424 0.00007
NM_000337.6(SGCD):c.630C>T (p.Ile210=) rs763051644 0.00002
NC_000005.10:g.156326901A>G rs915480419
NC_000005.10:g.156327060C>G rs1767843316
NM_000337.5(SGCD):c.-372C>G rs7717393
NM_000337.5(SGCD):c.-412A>T rs7724969
NM_000337.6(SGCD):c.-94C>G rs13170573
NM_000337.6(SGCD):c.105G>C (p.Leu35=) rs193922392
NM_000337.6(SGCD):c.193-74171C>A rs6556621
NM_000337.6(SGCD):c.193-87del rs71577199
NM_000337.6(SGCD):c.193-88_193-87del rs71577199
NM_000337.6(SGCD):c.295-242TG[17] rs113243314
NM_000337.6(SGCD):c.295-242TG[19] rs113243314
NM_000337.6(SGCD):c.295-242TG[20] rs113243314
NM_000337.6(SGCD):c.295-242TG[22] rs113243314
NM_000337.6(SGCD):c.295-242TG[23] rs113243314
NM_000337.6(SGCD):c.295-242TG[24] rs113243314
NM_000337.6(SGCD):c.3+19C>T rs182715924
NM_000337.6(SGCD):c.4-69dup rs80276463
NM_000337.6(SGCD):c.575+111_575+117del rs3832352
NM_000337.6(SGCD):c.576-133dup rs3215118
NM_000337.6(SGCD):c.699+11del rs2113178377
NM_000337.6(SGCD):c.699+12del rs2113178411
NM_000337.6(SGCD):c.699+13_699+15del rs397517924
NM_000337.6(SGCD):c.699+14del rs2113178436

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