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rs121917844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917844(C;T)
Make rs121917844(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position177994153
GenePROP1
is asnp
is mentioned by
dbSNPrs121917844
ebirs121917844
HLIrs121917844
Exacrs121917844
Varsomers121917844
Maprs121917844
PheGenIrs121917844
hapmaprs121917844
1000 genomesrs121917844
hgdprs121917844
ensemblrs121917844
gopubmedrs121917844
geneviewrs121917844
scholarrs121917844
googlers121917844
pharmgkbrs121917844
gwascentralrs121917844
openSNPrs121917844
23andMers121917844
23andMe allrs121917844
SNP Nexus

SNPshotrs121917844
SNPdbers121917844
MSV3drs121917844
GWAS Ctlgrs121917844
Max Magnitude0
ClinVar
Risk rs121917844(T;T)
Alt rs121917844(T;T)
Reference rs121917844(C;C)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421154G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008573.3,