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rs121917841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121917841(C;C)
Make rs121917841(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position177994185
GenePROP1
is asnp
is mentioned by
dbSNPrs121917841
ebirs121917841
HLIrs121917841
Exacrs121917841
Varsomers121917841
Maprs121917841
PheGenIrs121917841
hapmaprs121917841
1000 genomesrs121917841
hgdprs121917841
ensemblrs121917841
gopubmedrs121917841
geneviewrs121917841
scholarrs121917841
googlers121917841
pharmgkbrs121917841
gwascentralrs121917841
openSNPrs121917841
23andMers121917841
23andMe allrs121917841
SNP Nexus

SNPshotrs121917841
SNPdbers121917841
MSV3drs121917841
GWAS Ctlgrs121917841
Max Magnitude0
ClinVar
Risk rs121917841(C;C)
Alt rs121917841(C;C)
Reference rs121917841(T;T)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421186A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008568.3,