"Ambry Genetics"[submitter] AND "MIF"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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

ClinVar