Related gene-specific medical variations for Gene (Select 284889) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126460	NM_002415.2(MIF):c.220C>G (p.Arg74Gly)	MIF, MIF-AS1 (R74G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3060033	NM_002415.2(MIF):c.282-6C>G	MIF, MIF-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MIF-related condition	GBenign
Select item 3049829	NM_002415.2(MIF):c.224C>T (p.Ser75Phe)	MIF, MIF-AS1 (S75F)	Single nucleotide variant (non-coding transcript variant +1 more)	MIF-related condition	GLikely benign
Select item 3035802	NM_002415.2(MIF):c.204C>A (p.Ile68=)	MIF, MIF-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	MIF-related condition	GLikely benign
Select item 2652976	NM_002415.2(MIF):c.5C>G (p.Pro2Arg)	MIF, MIF-AS1 (P2R)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2598734	NM_002415.2(MIF):c.195C>G (p.Ile65Met)	MIF, MIF-AS1 (I65M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2543416	NM_002415.2(MIF):c.221G>T (p.Arg74Leu)	MIF, MIF-AS1 (R74L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2537629	NM_002415.2(MIF):c.142A>G (p.Met48Val)	MIF, MIF-AS1 (M48V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2388879	NM_002415.2(MIF):c.100C>A (p.Pro34Thr)	MIF, MIF-AS1 (P34T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2207622	NM_002415.2(MIF):c.83C>T (p.Ala28Val)	MIF, MIF-AS1 (A28V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 781909	NM_002415.2(MIF):c.282-9C>T	MIF, MIF-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 712657	NM_002415.2(MIF):c.282-7C>A	MIF, MIF-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 546911	NM_002415.2(MIF):c.172G>A (p.Ala58Thr)	MIF, MIF-AS1 (A58T)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance