List of variants in gene SDHC reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.77+32A>T	rs77828459	0.12254
NM_003001.5(SDHC):c.77+36T>A	rs117507008	0.04608
NM_003001.5(SDHC):c.-32T>C	rs115782155	0.01342
NM_003001.5(SDHC):c.354T>C (p.Phe118=)	rs61733156	0.00454
NM_003001.5(SDHC):c.406-8G>T	rs747093483

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