Related gene-specific medical variations for Gene (Select 10901) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3082090	NM_021004.4(DHRS4):c.94A>G (p.Asn32Asp)	DHRS4, DHRS4-AS1 (N32D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082081	NM_021004.4(DHRS4):c.206T>A (p.Val69Glu)	DHRS4, DHRS4-AS1 (V69E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3082080	NM_021004.4(DHRS4):c.197A>C (p.Gln66Pro)	DHRS4, DHRS4-AS1 (Q66P)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 2276284	NM_021004.4(DHRS4):c.71T>G (p.Met24Arg)	DHRS4, DHRS4-AS1 (M24R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275707	NM_021004.4(DHRS4):c.74C>T (p.Thr25Ile)	DHRS4, DHRS4-AS1 (T25I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275308	NM_021004.4(DHRS4):c.41G>C (p.Trp14Ser)	DHRS4, DHRS4-AS1 (W14S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790140	NM_021004.4(DHRS4):c.34C>A (p.Arg12=)	DHRS4, DHRS4-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 736886	NM_021004.4(DHRS4):c.191G>A (p.Arg64Gln)	DHRS4, DHRS4-AS1 (R64Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign