Related gene-specific medical variations for Gene (Select 2252) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278653	NM_002009.4(FGF7):c.190A>G (p.Ile64Val)	FAM227B, FGF7 (I64V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278652	NM_002009.4(FGF7):c.68G>T (p.Cys23Phe)	FAM227B, FGF7 (C23F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278651	NM_002009.4(FGF7):c.53G>A (p.Cys18Tyr)	FAM227B, FGF7 (C18Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278650	NM_002009.4(FGF7):c.58C>T (p.His20Tyr)	FAM227B, FGF7 (H20Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094755	NM_002009.4(FGF7):c.80C>G (p.Thr27Ser)	FAM227B, FGF7 (T27S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094754	NM_002009.4(FGF7):c.539A>C (p.Lys180Thr)	FAM227B, FGF7 (K180T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094753	NM_002009.4(FGF7):c.107C>T (p.Thr36Ile)	FAM227B, FGF7 (T36I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480711	NM_002009.4(FGF7):c.76G>T (p.Gly26Cys)	FAM227B, FGF7 (G26C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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