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rs864309519

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864309519(-;G)
Make rs864309519(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position43644771
GeneNNT
is asnp
is mentioned by
dbSNPrs864309519
ClinGenrs864309519
ebirs864309519
HLIrs864309519
Exacrs864309519
Varsomers864309519
Maprs864309519
PheGenIrs864309519
hapmaprs864309519
1000 genomesrs864309519
hgdprs864309519
ensemblrs864309519
gopubmedrs864309519
geneviewrs864309519
scholarrs864309519
googlers864309519
pharmgkbrs864309519
gwascentralrs864309519
openSNPrs864309519
23andMers864309519
23andMe allrs864309519
SNP Nexus

SNPshotrs864309519
SNPdbers864309519
MSV3drs864309519
GWAS Ctlgrs864309519
Max Magnitude0
ClinVar
Risk rs864309519(G;G)
Alt rs864309519(G;G)
Reference Rs864309519(-;-)
Significance Pathogenic
Disease Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency
Variation info
Gene NNT
CLNDBN Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency
Reversed 0
HGVS NC_000005.9:g.43644873dupG
CLNSRC
CLNACC RCV000202606.1,