Related gene-specific medical variations for Gene (Select 8609) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3238754	NM_003709.4(KLF7):c.419C>T (p.Ser140Leu)	KLF7 (S107L +2 more)	Single nucleotide variant (missense variant)	KLF7-related neurodevelopmental disorder	GUncertain significance
Select item 1325587	NM_001270943.2(KLF7):c.3+1G>T	KLF7	Single nucleotide variant (splice donor variant)	See cases	GUncertain significance
Select item 871305	NM_003709.4(KLF7):c.487A>C (p.Thr163Pro)	KLF7 (T130P +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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