Related gene-specific medical variations for Gene (Select 5733) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2559833	NM_198719.2(PTGER3):c.121C>G (p.Pro41Ala)	PTGER3, ZRANB2-AS1 (P41A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297485	NM_198719.2(PTGER3):c.64A>C (p.Thr22Pro)	ZRANB2-AS1, PTGER3 (T22P)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2224214	NM_198719.2(PTGER3):c.23G>A (p.Gly8Glu)	ZRANB2-AS1, PTGER3 (G8E)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 814094	GRCh37/hg19 1p31.1(chr1:71366112-71468493)x1	PTGER3	Copy number loss	not provided	GUncertain significance
Select item 777911	NM_198719.2(PTGER3):c.111C>G (p.Leu37=)	PTGER3, ZRANB2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 152784	GRCh38/hg38 1p31.1(chr1:70907033-70991687)x1	PTGER3	Copy number loss	See cases	GUncertain significance

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