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rs121917843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917843(C;T)
Make rs121917843(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position177994231
GenePROP1
is asnp
is mentioned by
dbSNPrs121917843
ebirs121917843
HLIrs121917843
Exacrs121917843
Varsomers121917843
Maprs121917843
PheGenIrs121917843
hapmaprs121917843
1000 genomesrs121917843
hgdprs121917843
ensemblrs121917843
gopubmedrs121917843
geneviewrs121917843
scholarrs121917843
googlers121917843
pharmgkbrs121917843
gwascentralrs121917843
openSNPrs121917843
23andMers121917843
23andMe allrs121917843
SNP Nexus

SNPshotrs121917843
SNPdbers121917843
MSV3drs121917843
GWAS Ctlgrs121917843
Max Magnitude0
ClinVar
Risk rs121917843(T;T)
Alt rs121917843(T;T)
Reference rs121917843(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.177421232G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008572.4,