C4551630[trait identifier] AND "Mendelics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 38918	NM_001099274.3(TINF2):c.841G>A (p.Glu281Lys)	TINF2, TGM1 (E281K +1 more)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 12496	NM_000359.3(TGM1):c.1552G>A (p.Val518Met)	TGM1 (V518M)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity