List of variants in gene SDHC reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	rs898854295	0.00003
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	rs587778661	0.00001
NM_003001.5(SDHC):c.214C>T (p.Arg72Cys)	rs756676111	0.00001
NM_003001.5(SDHC):c.215G>A (p.Arg72His)	rs778582853	0.00001
NM_003001.5(SDHC):c.380A>G (p.His127Arg)	rs786203457	0.00001
NM_003001.5(SDHC):c.405+1G>T	rs587776653	0.00001
NM_003001.5(SDHC):c.179+1G>C	rs1057517818
NM_003001.5(SDHC):c.21-2A>G	rs1131691062
NM_003001.5(SDHC):c.387G>A (p.Trp129Ter)	rs981049067
NM_003001.5(SDHC):c.406-1G>T
NM_003001.5(SDHC):c.439C>T (p.Gln147Ter)	rs1571898957
NM_003001.5(SDHC):c.78-2A>G

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