"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "NR1H4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1691436	NM_001206979.2(NR1H4):c.91G>T (p.Glu31Ter)	NR1H4 (E31* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GLikely pathogenic
Select item 1694078	NM_001206979.2(NR1H4):c.374A>G (p.Glu125Gly)	NR1H4 (E125G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2074373	NM_001206979.2(NR1H4):c.875C>T (p.Thr292Met)	NR1H4 (T241M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 502027	NM_001206979.2(NR1H4):c.1072A>C (p.Asn358His)	NR1H4 (N354H +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2683212	NM_001206979.2(NR1H4):c.1282C>G (p.Pro428Ala)	NR1H4 (P377A +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 594490	NM_001206979.2(NR1H4):c.1322T>C (p.Leu441Pro)	NR1H4 (L437P +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

ClinVar