C1840528[trait identifier] AND "GeneReviews"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65496	NM_003244.4(TGIF1):c.16+1845C>T	TGIF1	Single nucleotide variant (5 prime UTR variant +1 more)	Holoprosencephaly 4	GBenign
Select item 65507	NM_003244.4(TGIF1):c.581T>G (p.Val194Gly)	TGIF1 (V174G +3 more)	Single nucleotide variant (missense variant)	Holoprosencephaly 4	GBenign
Select item 65504	TGIF1:c.887C>T		Single nucleotide variant	Holoprosencephaly 4	GBenign

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