List of variants in gene SDHC reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.43C>T (p.Arg15Ter)	rs201286421	0.00002
NM_003001.5(SDHC):c.1A>G (p.Met1Val)	rs755235380	0.00001
NM_003001.5(SDHC):c.214C>T (p.Arg72Cys)	rs756676111	0.00001
NM_003001.5(SDHC):c.380A>G (p.His127Arg)	rs786203457	0.00001
NM_003001.5(SDHC):c.397C>T (p.Arg133Ter)	rs764575966	0.00001
NM_003001.5(SDHC):c.405+1G>T	rs587776653	0.00001
NM_003001.5(SDHC):c.17_18dup (p.Arg7Ter)	rs1553260596
NM_003001.5(SDHC):c.2T>G (p.Met1Arg)	rs1670517782
NM_003001.5(SDHC):c.3G>A (p.Met1Ile)	rs587776652

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