ClinVar Miner

List of variants in gene SDHC reported as benign for adrenal gland disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_003001.3(SDHC):c.*1025G>T rs16832859
NM_003001.3(SDHC):c.*1181_*1182insA rs34067216
NM_003001.3(SDHC):c.*123C>G rs3813632
NM_003001.3(SDHC):c.*1335A>G rs3935401
NM_003001.3(SDHC):c.*1379C>T rs114731359
NM_003001.3(SDHC):c.*1800G>C rs72714988
NM_003001.3(SDHC):c.*2052C>G rs12239492
NM_003001.3(SDHC):c.*2156A>C rs116668612
NM_003001.3(SDHC):c.*247C>G rs540126021
NM_003001.3(SDHC):c.*385G>A rs8266
NM_003001.3(SDHC):c.*469G>A rs148834287
NM_003001.3(SDHC):c.*612C>T rs16865495
NM_003001.3(SDHC):c.*624A>G rs114438179
NM_003001.3(SDHC):c.*84G>C rs201210474
NM_003001.3(SDHC):c.*968A>G rs4600063
NM_003001.3(SDHC):c.-32T>C rs115782155
NM_003001.3(SDHC):c.179+10G>A rs532455044
NM_003001.3(SDHC):c.354T>C (p.Phe118=) rs61733156

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