ClinVar Miner

List of variants in gene SDHC reported as uncertain significance for adrenal gland pheochromocytoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_003001.3(SDHC):c.*1012G>T rs886045484
NM_003001.3(SDHC):c.*1098T>C rs569588829
NM_003001.3(SDHC):c.*115T>G rs886045478
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.*174G>A rs886045479
NM_003001.3(SDHC):c.*1784G>C rs886045491
NM_003001.3(SDHC):c.*1843C>A rs886045492
NM_003001.3(SDHC):c.*1889T>C rs746551127
NM_003001.3(SDHC):c.*1898C>A rs886045493
NM_003001.3(SDHC):c.*1918G>A rs867593097
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.*2274G>A rs886045497
NM_003001.3(SDHC):c.*251C>T rs886045480
NM_003001.3(SDHC):c.*34A>G rs886045477
NM_003001.3(SDHC):c.*397G>A rs74124906
NM_003001.3(SDHC):c.*518G>A rs375109418
NM_003001.3(SDHC):c.*527G>T rs886045481
NM_003001.3(SDHC):c.*632A>G rs886045482
NM_003001.3(SDHC):c.*780G>A rs886045483
NM_003001.3(SDHC):c.15G>T (p.Leu5Phe) rs771746264
NM_003001.3(SDHC):c.21-10dup rs759481419
NM_003001.3(SDHC):c.406-13del rs752685687
NM_003001.3(SDHC):c.77+13G>C rs779727693
NM_003001.3(SDHC):c.8C>T (p.Ala3Val) rs142139022

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