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rs104893764

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893764(A;A)
Make rs104893764(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position87260082
GenePOU1F1
is asnp
is mentioned by
dbSNPrs104893764
ebirs104893764
HLIrs104893764
Exacrs104893764
Varsomers104893764
Maprs104893764
PheGenIrs104893764
hapmaprs104893764
1000 genomesrs104893764
hgdprs104893764
ensemblrs104893764
gopubmedrs104893764
geneviewrs104893764
scholarrs104893764
googlers104893764
pharmgkbrs104893764
gwascentralrs104893764
openSNPrs104893764
23andMers104893764
23andMe allrs104893764
SNP Nexus

SNPshotrs104893764
SNPdbers104893764
MSV3drs104893764
GWAS Ctlgrs104893764
Max Magnitude0
OMIM173110
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104893764(A;A)
Alt rs104893764(A;A)
Reference rs104893764(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.87309232C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014583.26,