Related gene-specific medical variations for Gene (Select 115409980) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2404758	NM_173157.3(NR4A1):c.1660C>T (p.Arg554Cys)	NR4A1, NR4A1AS (R608C +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2386019	NM_173157.3(NR4A1):c.1655T>C (p.Leu552Pro)	NR4A1, NR4A1AS (L552P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2351512	NM_173157.3(NR4A1):c.1688G>A (p.Arg563Gln)	NR4A1, NR4A1AS (R563Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220870	NM_173157.3(NR4A1):c.1633G>A (p.Glu545Lys)	NR4A1AS, NR4A1 (E558K +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance

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