Related gene-specific medical variations for Gene (Select 5732) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3311286	NM_000956.4(PTGER2):c.370A>G (p.Met124Val)	LOC130055639, PTGER2 (M124V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220719	NM_000956.4(PTGER2):c.482A>T (p.Tyr161Phe)	LOC130055639, PTGER2 (Y161F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220718	NM_000956.4(PTGER2):c.439C>T (p.Arg147Cys)	LOC130055639, PTGER2 (R147C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601262	NM_000956.4(PTGER2):c.647T>G (p.Phe216Cys)	LOC130055640, PTGER2 (F216C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277829	NM_000956.4(PTGER2):c.377T>C (p.Met126Thr)	LOC130055639, PTGER2 (M126T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218815	NM_000956.4(PTGER2):c.540G>C (p.Gln180His)	LOC130055640, PTGER2 (Q180H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 13360	NC_000014.9:g.52300623G>A	PTGER2	Single nucleotide variant	Asthma, aspirin-induced, susceptibility to	Grisk factor

ClinVar