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rs104893755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893755(C;T)
Make rs104893755(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87259959
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893755
ebirs104893755
HLIrs104893755
Exacrs104893755
Varsomers104893755
Maprs104893755
PheGenIrs104893755
hapmaprs104893755
1000 genomesrs104893755
hgdprs104893755
ensemblrs104893755
gopubmedrs104893755
geneviewrs104893755
scholarrs104893755
googlers104893755
pharmgkbrs104893755
gwascentralrs104893755
openSNPrs104893755
23andMers104893755
23andMe allrs104893755
SNP Nexus

SNPshotrs104893755
SNPdbers104893755
MSV3drs104893755
GWAS Ctlgrs104893755
Max Magnitude0
OMIM173110
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893755(T;T)
Alt rs104893755(T;T)
Reference rs104893755(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.87309109G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014573.26,