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rs606231411

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs606231411(C;T)
Make rs606231411(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position87310484
is asnp
is mentioned by
dbSNPrs606231411
ebirs606231411
HLIrs606231411
Exacrs606231411
Varsomers606231411
Maprs606231411
PheGenIrs606231411
hapmaprs606231411
1000 genomesrs606231411
hgdprs606231411
ensemblrs606231411
gopubmedrs606231411
geneviewrs606231411
scholarrs606231411
googlers606231411
pharmgkbrs606231411
gwascentralrs606231411
openSNPrs606231411
23andMers606231411
23andMe allrs606231411
SNP Nexus

SNPshotrs606231411
SNPdbers606231411
MSV3drs606231411
GWAS Ctlgrs606231411
Max Magnitude0
ClinVar
Risk rs606231411(T;T)
Alt rs606231411(T;T)
Reference rs606231411(C;C)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 0
HGVS NC_000003.12:g.87310484C>T
CLNSRC
CLNACC RCV000148937.1,