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rs104893761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893761(G;G)
Make rs104893761(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87264323
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893761
ebirs104893761
HLIrs104893761
Exacrs104893761
Varsomers104893761
Maprs104893761
PheGenIrs104893761
hapmaprs104893761
1000 genomesrs104893761
hgdprs104893761
ensemblrs104893761
gopubmedrs104893761
geneviewrs104893761
scholarrs104893761
googlers104893761
pharmgkbrs104893761
gwascentralrs104893761
openSNPrs104893761
23andMers104893761
23andMe allrs104893761
SNP Nexus

SNPshotrs104893761
SNPdbers104893761
MSV3drs104893761
GWAS Ctlgrs104893761
Max Magnitude0
OMIM173110
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104893761(G;G)
Alt rs104893761(G;G)
Reference rs104893761(T;T)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene POU1F1
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 1
HGVS NC_000003.11:g.87313473A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014578.27,