List of variants in gene SDHD 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_003002.4(SDHD):c.315-32T>C	rs4151637	0.11444
NM_003002.4(SDHD):c.170-29A>G	rs9919624	0.11431
NM_003002.4(SDHD):c.204C>T (p.Ser68=)	rs9919552	0.11428
NM_003002.4(SDHD):c.312C>T (p.His104=)	rs61734352	0.00690
NM_003002.4(SDHD):c.149A>G (p.His50Arg)	rs11214077	0.00679

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