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rs104893765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893765(A;A)
Make rs104893765(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position87262160
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893765
ebirs104893765
HLIrs104893765
Exacrs104893765
Varsomers104893765
Maprs104893765
PheGenIrs104893765
hapmaprs104893765
1000 genomesrs104893765
hgdprs104893765
ensemblrs104893765
gopubmedrs104893765
geneviewrs104893765
scholarrs104893765
googlers104893765
pharmgkbrs104893765
gwascentralrs104893765
openSNPrs104893765
23andMers104893765
23andMe allrs104893765
SNP Nexus

SNPshotrs104893765
SNPdbers104893765
MSV3drs104893765
GWAS Ctlgrs104893765
Max Magnitude0
OMIM173110
Desc
Variant0013
Relatedalso
ClinVar
Risk rs104893765(A;A)
Alt rs104893765(A;A)
Reference rs104893765(G;G)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene POU1F1
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 1
HGVS NC_000003.11:g.87311310C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014584.25,