Related gene-specific medical variations for Gene (Select 26098) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3087213	NM_001202438.2(EDRF1):c.3124G>T (p.Val1042Phe)	EDRF1, EDRF1-AS1 (V1008F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2620696	NM_001202438.2(EDRF1):c.3136C>A (p.His1046Asn)	EDRF1, EDRF1-AS1 (H1012N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2605667	NM_001202438.2(EDRF1):c.2798G>C (p.Gly933Ala)	EDRF1, EDRF1-AS1 (G899A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556348	NM_001202438.2(EDRF1):c.2809A>T (p.Asn937Tyr)	EDRF1, EDRF1-AS1 (N937Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244518	NM_001202438.2(EDRF1):c.2777G>C (p.Arg926Pro)	EDRF1, EDRF1-AS1 (R926P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231422	NM_001202438.2(EDRF1):c.2614G>A (p.Glu872Lys)	EDRF1, EDRF1-AS1 (E838K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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