Related gene-specific medical variations for Gene (Select 130055420) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3292198	NM_019839.5(LTB4R2):c.385G>T (p.Ala129Ser)	CIDEB, LOC130055420 +1 more (A129S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121391	NM_019839.5(LTB4R2):c.392G>A (p.Arg131Gln)	CIDEB, LOC130055420 +1 more (R131Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121390	NM_019839.5(LTB4R2):c.391C>T (p.Arg131Trp)	CIDEB, LOC130055420 +1 more (R131W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534260	NM_019839.5(LTB4R2):c.338G>C (p.Gly113Ala)	CIDEB, LOC130055420 +1 more (G113A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534259	NM_019839.5(LTB4R2):c.337G>T (p.Gly113Cys)	LTB4R2, CIDEB +1 more (G113C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2356853	NM_019839.5(LTB4R2):c.376C>T (p.Pro126Ser)	CIDEB, LOC130055420 +1 more (P126S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 712146	NM_019839.5(LTB4R2):c.388C>T (p.Pro130Ser)	CIDEB, LOC130055420 +1 more (P130S)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

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