List of variants in gene SDHD reported as benign by GeneDx

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_003002.4(SDHD):c.315-1669A>G	rs592626	0.99043
NM_003002.4(SDHD):c.315-1490T>C	rs10749989	0.43335
NM_003002.4(SDHD):c.315-32T>C	rs4151637	0.11444
NM_003002.4(SDHD):c.315-239G>A	rs7122054	0.11432
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.315-1646C>T	rs111659413	0.10719
NM_003002.4(SDHD):c.315-1402C>G	rs370667125	0.04800
NM_003002.4(SDHD):c.315-1405del	rs111885447	0.04791
NM_003002.4(SDHD):c.*260T>A	rs149570245	0.04112
NM_003002.4(SDHD):c.315-1708C>T	rs113458823	0.02846
NM_003002.4(SDHD):c.170-270T>A	rs73568085	0.02800
NM_003002.4(SDHD):c.314+124T>C	rs118074328	0.00706
NM_003002.4(SDHD):c.312C>T (p.His104=)	rs61734352	0.00690
NM_003002.4(SDHD):c.149A>G (p.His50Arg)	rs11214077	0.00679
NM_003002.4(SDHD):c.169+244del	rs11315004

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