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rs587776798

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776798(-;-)
Make rs587776798(-;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position87260023
GenePOU1F1
is asnp
is mentioned by
dbSNPrs587776798
ebirs587776798
HLIrs587776798
Exacrs587776798
Varsomers587776798
Maprs587776798
PheGenIrs587776798
hapmaprs587776798
1000 genomesrs587776798
hgdprs587776798
ensemblrs587776798
gopubmedrs587776798
geneviewrs587776798
scholarrs587776798
googlers587776798
pharmgkbrs587776798
gwascentralrs587776798
openSNPrs587776798
23andMers587776798
23andMe allrs587776798
SNP Nexus

SNPshotrs587776798
SNPdbers587776798
MSV3drs587776798
GWAS Ctlgrs587776798
Max Magnitude0
ClinVar
Risk rs587776798(;)
Alt rs587776798(;)
Reference rs587776798(T;T)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene POU1F1
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 0
HGVS NC_000003.11:g.87309173delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000014580.27,