List of variants in gene NR1H4 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001206979.2(NR1H4):c.1072A>C (p.Asn358His)	rs149287629	0.00035
NM_001206979.2(NR1H4):c.875C>T (p.Thr292Met)	rs748378207	0.00006
NM_001206979.2(NR1H4):c.1322T>C (p.Leu441Pro)	rs745674560	0.00001
NM_001206979.2(NR1H4):c.1282C>G (p.Pro428Ala)	rs1955516556
NM_001206979.2(NR1H4):c.374A>G (p.Glu125Gly)	rs2136158932
NM_001206979.2(NR1H4):c.91G>T (p.Glu31Ter)	rs753528227

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