List of variants in gene SDHC reported as benign for benign neoplasm

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003001.4(SDHC):c.1181_1182insA	rs34067216	0.11567
NM_003001.5(SDHC):c.-32T>C	rs115782155	0.01342

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