List of variants in gene NR4A2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006186.4(NR4A2):c.732C>A (p.Leu244=)	rs16840266	0.00110
NM_006186.4(NR4A2):c.289A>G (p.Met97Val)	rs143618355	0.00011
NM_006186.4(NR4A2):c.657T>C (p.Ala219=)	rs769677341	0.00006
NM_006186.4(NR4A2):c.659_661del	rs577936871
NM_006186.4(NR4A2):c.1287C>T (p.Asp429=)

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