List of variants in gene combination NR0B2, NUDC reported as uncertain significance for Obesity

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021969.3(NR0B2):c.473G>A (p.Ser158Asn)	rs151014108	0.00413
NM_021969.3(NR0B2):c.712C>T (p.Arg238Cys)	rs777140276	0.00001
NM_021969.3(NR0B2):c.528C>A (p.Asn176Lys)	rs757929402

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