"PreventionGenetics, part of Exact Sciences"[submitter] AND "KLF7"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2637281	NM_003709.4(KLF7):c.398T>G (p.Val133Gly)	KLF7 (V100G +2 more)	Single nucleotide variant (missense variant)	KLF7-related disorder	GUncertain significance
Select item 3053114	NM_003709.4(KLF7):c.393C>T (p.Asn131=)	KLF7	Single nucleotide variant (synonymous variant)	KLF7-related disorder	GLikely benign
Select item 3051378	NM_003709.4(KLF7):c.372C>T (p.Ala124=)	KLF7	Single nucleotide variant (synonymous variant)	KLF7-related disorder	GLikely benign
Select item 789158	NM_003709.4(KLF7):c.246C>T (p.Leu82=)	KLF7	Single nucleotide variant (synonymous variant)	KLF7-related disorder +1 more	GBenign/Likely benign
Select item 3041596	NM_003709.4(KLF7):c.171C>T (p.Asp57=)	KLF7	Single nucleotide variant (synonymous variant)	KLF7-related disorder	GBenign
Select item 3059981	NM_003709.4(KLF7):c.103-9672G>A	KLF7	Single nucleotide variant (synonymous variant +1 more)	KLF7-related disorder	GBenign

ClinVar