List of variants in gene SDHD reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.*613T>C	rs693441	0.93280
NM_003002.4(SDHD):c.204C>T (p.Ser68=)	rs9919552	0.11428
NM_003002.4(SDHD):c.*803A>G	rs17113461	0.10714
NM_003002.4(SDHD):c.*260T>A	rs149570245	0.04112

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