C3494181[trait identifier] AND "Genetics and Molecular Pathology, SA P - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 6903	NM_003002.4(SDHD):c.64C>T (p.Arg22Ter)	SDHD (R22*)	Single nucleotide variant (nonsense +2 more)	not provided +6 more	GPathogenic
Select item 6893	NM_003002.4(SDHD):c.112C>T (p.Arg38Ter)	SDHD (R38*)	Single nucleotide variant (nonsense +2 more)	Hereditary cancer-predisposing syndrome +6 more	GPathogenic
Select item 6896	NM_003002.4(SDHD):c.242C>T (p.Pro81Leu)	SDHD (P81L +1 more)	Single nucleotide variant (missense variant +2 more)	Hereditary cancer-predisposing syndrome +9 more	GPathogenic/Likely pathogenic

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