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rs387907233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907233(C;C)
Make rs387907233(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position43700172
GeneNNT
is asnp
is mentioned by
dbSNPrs387907233
ebirs387907233
HLIrs387907233
Exacrs387907233
Varsomers387907233
Maprs387907233
PheGenIrs387907233
hapmaprs387907233
1000 genomesrs387907233
hgdprs387907233
ensemblrs387907233
gopubmedrs387907233
geneviewrs387907233
scholarrs387907233
googlers387907233
pharmgkbrs387907233
gwascentralrs387907233
openSNPrs387907233
23andMers387907233
23andMe allrs387907233
SNP Nexus

SNPshotrs387907233
SNPdbers387907233
MSV3drs387907233
GWAS Ctlgrs387907233
Max Magnitude0
ClinVar
Risk rs387907233(C;C)
Alt rs387907233(C;C)
Reference rs387907233(T;T)
Significance Pathogenic
Disease Glucocorticoid deficiency 4
Variation info
Gene NNT
CLNDBN Glucocorticoid deficiency 4
Reversed 0
HGVS NC_000005.9:g.43700274T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000029195.3,