ClinVar Miner

List of variants in gene SDHC reported as likely benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_003001.5(SDHC):c.77+32A>T rs77828459 0.12254
NM_003001.5(SDHC):c.*78G>A rs182629842 0.00182
NM_003001.5(SDHC):c.77+31T>A rs759799321 0.00056
NM_003001.5(SDHC):c.20+22G>C rs182261879 0.00032
NM_003001.5(SDHC):c.120G>A (p.Arg40=) rs36097930 0.00020
NM_003001.5(SDHC):c.405+13G>A rs369274171 0.00008
NM_003001.5(SDHC):c.179+10G>A rs532455044 0.00006
NM_003001.5(SDHC):c.*45C>A rs370435919 0.00004
NM_003001.5(SDHC):c.180-47G>A rs762913083 0.00002
NM_003001.5(SDHC):c.*38T>C
NM_003001.5(SDHC):c.-14G>C
NM_003001.5(SDHC):c.20+42G>A
NM_003001.5(SDHC):c.21-14C>T rs1450437203
NM_003001.5(SDHC):c.242-20C>T
NM_003001.5(SDHC):c.242-37T>C rs765053466
NM_003001.5(SDHC):c.242-3C>T
NM_003001.5(SDHC):c.242-40T>A
NM_003001.5(SDHC):c.242-9del
NM_003001.5(SDHC):c.405+36A>G
NM_003001.5(SDHC):c.406-13G>A rs758615918
NM_003001.5(SDHC):c.406-14T>G
NM_003001.5(SDHC):c.406-43T>G
NM_003001.5(SDHC):c.66C>G (p.Leu22=) rs778965036
NM_003001.5(SDHC):c.77+26_77+27insA
NM_003001.5(SDHC):c.77+31dup rs371604278
NM_003001.5(SDHC):c.77+32A>G
NM_003001.5(SDHC):c.77+32_77+33del rs751651691
NM_003001.5(SDHC):c.77+32del

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