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rs121909726

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909726(A;T)
Make rs121909726(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position143281964
GeneNR3C1
is asnp
is mentioned by
dbSNPrs121909726
ebirs121909726
HLIrs121909726
Exacrs121909726
Varsomers121909726
Maprs121909726
PheGenIrs121909726
hapmaprs121909726
1000 genomesrs121909726
hgdprs121909726
ensemblrs121909726
gopubmedrs121909726
geneviewrs121909726
scholarrs121909726
googlers121909726
pharmgkbrs121909726
gwascentralrs121909726
openSNPrs121909726
23andMers121909726
23andMe allrs121909726
SNP Nexus

SNPshotrs121909726
SNPdbers121909726
MSV3drs121909726
GWAS Ctlgrs121909726
Max Magnitude0
OMIM138040
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909726(T;T)
Alt rs121909726(T;T)
Reference rs121909726(A;A)
Significance Pathogenic
Disease Glucocorticoid resistance
Variation info
Gene NR3C1
CLNDBN Glucocorticoid resistance, cellular
Reversed 1
HGVS NC_000005.9:g.142661529T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017531.24,