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rs104893766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893766(C;G)
Make rs104893766(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position87262138
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893766
ebirs104893766
HLIrs104893766
Exacrs104893766
Varsomers104893766
Maprs104893766
PheGenIrs104893766
hapmaprs104893766
1000 genomesrs104893766
hgdprs104893766
ensemblrs104893766
gopubmedrs104893766
geneviewrs104893766
scholarrs104893766
googlers104893766
pharmgkbrs104893766
gwascentralrs104893766
openSNPrs104893766
23andMers104893766
23andMe allrs104893766
SNP Nexus

SNPshotrs104893766
SNPdbers104893766
MSV3drs104893766
GWAS Ctlgrs104893766
Max Magnitude0
OMIM173110
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104893766(G;G)
Alt rs104893766(G;G)
Reference rs104893766(C;C)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene POU1F1
CLNDBN Pituitary hormone deficiency, combined 1
Reversed 1
HGVS NC_000003.11:g.87311288G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014586.27,