"Ambry Genetics"[submitter] AND "DHRS4-AS1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2275308	NM_021004.4(DHRS4):c.41G>C (p.Trp14Ser)	DHRS4-AS1, DHRS4 (W14S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2462622	NM_021004.4(DHRS4):c.56T>G (p.Met19Arg)	DHRS4, DHRS4-AS1 (M19R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2600062	NM_021004.4(DHRS4):c.59C>T (p.Ala20Val)	DHRS4, DHRS4-AS1 (A20V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2276284	NM_021004.4(DHRS4):c.71T>G (p.Met24Arg)	DHRS4-AS1, DHRS4 (M24R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2275707	NM_021004.4(DHRS4):c.74C>T (p.Thr25Ile)	DHRS4-AS1, DHRS4 (T25I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2531960	NM_021004.4(DHRS4):c.149G>A (p.Arg50Gln)	DHRS4, DHRS4-AS1 (R50Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar