ClinVar Miner

List of variants in gene SDHC reported as uncertain significance for benign endocrine neoplasm

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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NM_003001.3(SDHC):c.*1012G>T rs886045484
NM_003001.3(SDHC):c.*1098T>C rs569588829
NM_003001.3(SDHC):c.*1314C>A rs376293449
NM_003001.3(SDHC):c.*1332C>A rs886045485
NM_003001.3(SDHC):c.*1481G>A rs886045486
NM_003001.3(SDHC):c.*1534G>T rs886045487
NM_003001.3(SDHC):c.*1584C>G rs886045488
NM_003001.3(SDHC):c.*1695G>T rs886045489
NM_003001.3(SDHC):c.*1699A>G rs886045490
NM_003001.3(SDHC):c.*1784G>C rs886045491
NM_003001.3(SDHC):c.*1843C>A rs886045492
NM_003001.3(SDHC):c.*1898C>A rs886045493
NM_003001.3(SDHC):c.*2141C>A rs886045494
NM_003001.3(SDHC):c.*2236C>A rs886045495
NM_003001.3(SDHC):c.*2264G>T rs886045496
NM_003001.3(SDHC):c.21-10dup rs759481419
NM_003001.3(SDHC):c.406-13del rs752685687
NM_003001.5(SDHC):c.*397G>A rs74124906
NM_003001.5(SDHC):c.*518G>A rs375109418
NM_003001.5(SDHC):c.*527G>T rs886045481
NM_003001.5(SDHC):c.8C>T (p.Ala3Val) rs142139022

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