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rs121917839

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917839(C;T)
Make rs121917839(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position177993032
GenePROP1
is asnp
is mentioned by
dbSNPrs121917839
ebirs121917839
HLIrs121917839
Exacrs121917839
Varsomers121917839
Maprs121917839
PheGenIrs121917839
hapmaprs121917839
1000 genomesrs121917839
hgdprs121917839
ensemblrs121917839
gopubmedrs121917839
geneviewrs121917839
scholarrs121917839
googlers121917839
pharmgkbrs121917839
gwascentralrs121917839
openSNPrs121917839
23andMers121917839
23andMe allrs121917839
SNP Nexus

SNPshotrs121917839
SNPdbers121917839
MSV3drs121917839
GWAS Ctlgrs121917839
Max Magnitude0
ClinVar
Risk rs121917839(T;T)
Alt rs121917839(T;T)
Reference rs121917839(C;C)
Significance Other
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177420033G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008563.7,