"Institute for Clinical Genetics, University Hospital TU Dresden, Univ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 392110	NM_017841.4(SDHAF2):c.-1A>C	SDHAF2	Single nucleotide variant (5 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 532518	NM_017841.4(SDHAF2):c.98G>A (p.Arg33His)	SDHAF2 (R33H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 576139	NM_017841.4(SDHAF2):c.194C>T (p.Thr65Ile)	SDHAF2 (T65I)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

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