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rs387907232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907232(C;T)
Make rs387907232(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position43649300
GeneNNT
is asnp
is mentioned by
dbSNPrs387907232
ebirs387907232
HLIrs387907232
Exacrs387907232
Varsomers387907232
Maprs387907232
PheGenIrs387907232
hapmaprs387907232
1000 genomesrs387907232
hgdprs387907232
ensemblrs387907232
gopubmedrs387907232
geneviewrs387907232
scholarrs387907232
googlers387907232
pharmgkbrs387907232
gwascentralrs387907232
openSNPrs387907232
23andMers387907232
23andMe allrs387907232
SNP Nexus

SNPshotrs387907232
SNPdbers387907232
MSV3drs387907232
GWAS Ctlgrs387907232
Max Magnitude0
ClinVar
Risk rs387907232(T;T)
Alt rs387907232(T;T)
Reference rs387907232(C;C)
Significance Pathogenic
Disease Glucocorticoid deficiency 4
Variation info
Gene NNT
CLNDBN Glucocorticoid deficiency 4
Reversed 0
HGVS NC_000005.9:g.43649402C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000029193.3,