List of variants in gene NR3C2 reported by Fulgent Genetics, Fulgent Genetics

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000901.5(NR3C2):c.2139T>C (p.Pro713=)	rs151096115	0.00862
NM_000901.5(NR3C2):c.1791A>G (p.Ser597=)	rs34905604	0.00366
NM_000901.5(NR3C2):c.1898-4T>C	rs72653856	0.00297
NM_000901.5(NR3C2):c.1398T>C (p.Tyr466=)	rs5524	0.00031
NM_000901.5(NR3C2):c.1172A>G (p.Gln391Arg)	rs569010694	0.00005
NM_000901.5(NR3C2):c.1824T>C (p.Asp608=)	rs557002204	0.00005
NM_000901.5(NR3C2):c.405G>C (p.Gln135His)	rs138893620	0.00004
NM_000901.5(NR3C2):c.334G>C (p.Val112Leu)	rs1330903694	0.00002
NM_000901.5(NR3C2):c.1513G>A (p.Glu505Lys)	rs774066754	0.00001
NM_000901.5(NR3C2):c.1951C>T (p.Arg651Ter)	rs1131691921
NM_000901.5(NR3C2):c.2839C>T (p.Arg947Ter)	rs121912569
NM_000901.5(NR3C2):c.934A>G (p.Ser312Gly)	rs1750038176

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.