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rs121917845

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917845(A;A)
Make rs121917845(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position177992808
GenePROP1
is asnp
is mentioned by
dbSNPrs121917845
ebirs121917845
HLIrs121917845
Exacrs121917845
Varsomers121917845
Maprs121917845
PheGenIrs121917845
hapmaprs121917845
1000 genomesrs121917845
hgdprs121917845
ensemblrs121917845
gopubmedrs121917845
geneviewrs121917845
scholarrs121917845
googlers121917845
pharmgkbrs121917845
gwascentralrs121917845
openSNPrs121917845
23andMers121917845
23andMe allrs121917845
SNP Nexus

SNPshotrs121917845
SNPdbers121917845
MSV3drs121917845
GWAS Ctlgrs121917845
Max Magnitude0
ClinVar
Risk rs121917845(A;A)
Alt rs121917845(A;A)
Reference rs121917845(G;G)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177419809C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008575.3,