ClinVar Miner

List of variants in gene SDHC reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
Download table as spreadsheet
HGVS dbSNP
NM_003001.3(SDHC):c.*1190T>A rs549554302
NM_003001.3(SDHC):c.*1191A>T rs566186299
NM_003001.3(SDHC):c.*1323G>A rs72714986
NM_003001.3(SDHC):c.*1378T>C rs116141910
NM_003001.3(SDHC):c.*1693G>A rs191417790
NM_003001.3(SDHC):c.*1731G>A rs115718047
NM_003001.3(SDHC):c.*2111C>T rs115166758
NM_003001.3(SDHC):c.*409G>A rs186995249
NM_003001.3(SDHC):c.*685C>T rs138085670
NM_003001.3(SDHC):c.*78G>A rs182629842
NM_003001.3(SDHC):c.*84G>C rs201210474
NM_003001.3(SDHC):c.*863G>A rs570400725
NM_003001.3(SDHC):c.120G>A (p.Arg40=) rs36097930
NM_003001.3(SDHC):c.162C>A (p.Pro54=) rs374450282
NM_003001.3(SDHC):c.179+10G>A rs532455044
NM_003001.3(SDHC):c.20+10G>A rs1060504224
NM_003001.3(SDHC):c.20+22G>C rs182261879
NM_003001.3(SDHC):c.20+7T>G rs1553260599
NM_003001.3(SDHC):c.241+7A>G rs878854586
NM_003001.3(SDHC):c.24C>T (p.His8=) rs761381438
NM_003001.3(SDHC):c.282G>A (p.Gly94=) rs536197277
NM_003001.3(SDHC):c.294T>C (p.Ser98=) rs376292127
NM_003001.3(SDHC):c.309G>A (p.Val103=) rs768273090
NM_003001.3(SDHC):c.30T>C (p.Gly10=) rs1170595036
NM_003001.3(SDHC):c.333A>G (p.Ala111=) rs950221552
NM_003001.3(SDHC):c.342C>T (p.His114=) rs143730978
NM_003001.3(SDHC):c.372C>T (p.Leu124=) rs766007157
NM_003001.3(SDHC):c.402C>T (p.His134=) rs754213041
NM_003001.3(SDHC):c.405+23C>T rs373731336
NM_003001.3(SDHC):c.406-10T>G rs1060504225
NM_003001.3(SDHC):c.406-8G>T rs747093483
NM_003001.3(SDHC):c.420A>G (p.Gly140=) rs794727791
NM_003001.3(SDHC):c.42C>T (p.Leu14=) rs1331533952
NM_003001.3(SDHC):c.465C>G (p.Val155=) rs1060504223
NM_003001.3(SDHC):c.466C>T (p.Leu156=) rs1553266500
NM_003001.3(SDHC):c.489T>C (p.Ser163=) rs559747670
NM_003001.3(SDHC):c.490A>T (p.Met164Leu) rs200375156
NM_003001.3(SDHC):c.66C>G (p.Leu22=) rs778965036
NM_003001.3(SDHC):c.6T>C (p.Ala2=) rs775353334
NM_003001.3(SDHC):c.81T>C (p.Ala27=) rs876659297
NM_003001.3(SDHC):c.99G>T (p.Thr33=) rs145535502

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.