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rs104893760

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893760(G;T)
Make rs104893760(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position87260022
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893760
ebirs104893760
HLIrs104893760
Exacrs104893760
Varsomers104893760
Maprs104893760
PheGenIrs104893760
hapmaprs104893760
1000 genomesrs104893760
hgdprs104893760
ensemblrs104893760
gopubmedrs104893760
geneviewrs104893760
scholarrs104893760
googlers104893760
pharmgkbrs104893760
gwascentralrs104893760
openSNPrs104893760
23andMers104893760
23andMe allrs104893760
SNP Nexus

SNPshotrs104893760
SNPdbers104893760
MSV3drs104893760
GWAS Ctlgrs104893760
Max Magnitude0
OMIM173110
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104893760(T;T)
Alt rs104893760(T;T)
Reference rs104893760(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.87309172C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014577.25,