Rs104893912

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893912(C;C)
Make rs104893912(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position143281905
GeneNR3C1
is asnp
is mentioned by
dbSNPrs104893912
Exacrs104893912
PheGenIrs104893912
nextbiors104893912
hapmaprs104893912
1000 genomesrs104893912
hgdprs104893912
ensemblrs104893912
gopubmedrs104893912
geneviewrs104893912
scholarrs104893912
googlers104893912
pharmgkbrs104893912
gwascentralrs104893912
openSNPrs104893912
23andMers104893912
23andMe allrs104893912
SNP Nexus

SNPshotrs104893912
SNPdbers104893912
MSV3drs104893912
Max Magnitude0
OMIM138040
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104893912(C;C)
Alt rs104893912(C;C)
Reference rs104893912(T;T)
Significance Pathogenic
Disease Glucocorticoid resistance
Variation info
Gene NR3C1
CLNDBN Glucocorticoid resistance, generalized
Reversed 1
HGVS NC_000005.9:g.142661470A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017538.26,