Variant (rsID / SNP)

rs6190

rs6190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NR3C1. Location: chromosome 5, position 142,780,337. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NR3C1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:142780337
Cytoband: 5q31.3
HGVS: NM_000176.3(NR3C1):c.68G>A (p.Arg23Lys)
Allele change: Silent

Associated conditions / phenotypes

Glucocorticoid resistance

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.