ClinVar Miner

List of variants in gene SGCD reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_000337.6(SGCD):c.*6717G>A rs1827368 0.90216
NM_000337.6(SGCD):c.84T>C (p.Tyr28=) rs1801193 0.39558
NM_000337.6(SGCD):c.*1527C>T rs284445 0.26081
NM_000337.6(SGCD):c.*3772dup rs397841758 0.20069
NM_000337.6(SGCD):c.*5863C>T rs11953631 0.15411
NM_000337.6(SGCD):c.*4395A>T rs10041876 0.15385
NM_000337.6(SGCD):c.*781G>C rs3857412 0.14424
NM_000337.6(SGCD):c.*1618T>C rs1389818 0.14033
NM_000337.6(SGCD):c.*4813T>C rs1845479 0.14018
NM_000337.6(SGCD):c.*4092A>G rs56389540 0.09897
NM_000337.6(SGCD):c.*5114C>T rs3913482 0.09173
NM_000337.6(SGCD):c.*7814C>T rs56233900 0.08817
NM_000337.6(SGCD):c.*3650G>T rs72803044 0.08674
NM_000337.6(SGCD):c.*1373A>G rs72803041 0.08567
NM_000337.6(SGCD):c.*2365T>C rs72803042 0.08564
NM_000337.6(SGCD):c.*360A>G rs72803040 0.08563
NM_000337.6(SGCD):c.*5990T>A rs72803047 0.08555
NM_000337.6(SGCD):c.*2712T>C rs56293630 0.08538
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.*6665G>A rs61633788 0.07733
NM_000337.6(SGCD):c.*4166T>C rs55653598 0.06787
NM_000337.6(SGCD):c.*3413G>C rs72803043 0.06785
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.290G>A (p.Arg97Gln) rs45559835 0.04292
NM_000337.6(SGCD):c.*4498G>A rs73304958 0.03775
NM_000337.6(SGCD):c.*363C>T rs6886827 0.03518
NM_000337.6(SGCD):c.*7596A>G rs80115276 0.02244
NM_000337.6(SGCD):c.*4895G>A rs115905727 0.01801
NM_000337.6(SGCD):c.*6400C>T rs10065295 0.01333
NM_000337.6(SGCD):c.*3898C>T rs74717343 0.01308
NM_000337.6(SGCD):c.*4818G>A rs76466586 0.01301
NM_000337.6(SGCD):c.*7816G>A rs78589560 0.00921
NM_000337.5(SGCD):c.-179A>G rs77808502 0.00918
NM_000337.6(SGCD):c.*6875G>A rs74370429 0.00888
NM_000337.6(SGCD):c.507G>A (p.Ala169=) rs10071079 0.00680
NM_000337.6(SGCD):c.*8071A>G rs73813790 0.00573
NM_000337.6(SGCD):c.*5877C>A rs117879283 0.00430
NM_000337.6(SGCD):c.*7866G>A rs115728448 0.00408
NM_000337.6(SGCD):c.*5226G>A rs552358256 0.00051
NM_000337.6(SGCD):c.-94C>G rs13170573

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