Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205344

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205344(-;-)
Make rs786205344(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position43619031
GeneNNT
is asnp
is mentioned by
dbSNPrs786205344
ebirs786205344
HLIrs786205344
Exacrs786205344
Varsomers786205344
Maprs786205344
PheGenIrs786205344
hapmaprs786205344
1000 genomesrs786205344
hgdprs786205344
ensemblrs786205344
gopubmedrs786205344
geneviewrs786205344
scholarrs786205344
googlers786205344
pharmgkbrs786205344
gwascentralrs786205344
openSNPrs786205344
23andMers786205344
23andMe allrs786205344
SNP Nexus

SNPshotrs786205344
SNPdbers786205344
MSV3drs786205344
GWAS Ctlgrs786205344
Max Magnitude0
ClinVar
Risk rs786205344(;)
Alt rs786205344(;)
Reference rs786205344(G;G)
Significance Pathogenic
Disease Glucocorticoid deficiency 4
Variation info
Gene NNT
CLNDBN Glucocorticoid deficiency 4
Reversed 0
HGVS NC_000005.9:g.43619133delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000029194.4,