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rs104893763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893763(A;T)
Make rs104893763(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87264294
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893763
ebirs104893763
HLIrs104893763
Exacrs104893763
Varsomers104893763
Maprs104893763
PheGenIrs104893763
hapmaprs104893763
1000 genomesrs104893763
hgdprs104893763
ensemblrs104893763
gopubmedrs104893763
geneviewrs104893763
scholarrs104893763
googlers104893763
pharmgkbrs104893763
gwascentralrs104893763
openSNPrs104893763
23andMers104893763
23andMe allrs104893763
SNP Nexus

SNPshotrs104893763
SNPdbers104893763
MSV3drs104893763
GWAS Ctlgrs104893763
Max Magnitude0
OMIM173110
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104893763(T;T)
Alt rs104893763(T;T)
Reference rs104893763(A;A)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene POU1F1
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 1
HGVS NC_000003.11:g.87313444T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014582.27,