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rs121917840

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121917840(A;A)
Make rs121917840(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position177993041
GenePROP1
is asnp
is mentioned by
dbSNPrs121917840
ebirs121917840
HLIrs121917840
Exacrs121917840
Varsomers121917840
Maprs121917840
PheGenIrs121917840
hapmaprs121917840
1000 genomesrs121917840
hgdprs121917840
ensemblrs121917840
gopubmedrs121917840
geneviewrs121917840
scholarrs121917840
googlers121917840
pharmgkbrs121917840
gwascentralrs121917840
openSNPrs121917840
23andMers121917840
23andMe allrs121917840
SNP Nexus

SNPshotrs121917840
SNPdbers121917840
MSV3drs121917840
GWAS Ctlgrs121917840
Max Magnitude0
ClinVar
Risk rs121917840(A,C;A,C)
Alt rs121917840(A,C;A,C)
Reference rs121917840(T;T)
Significance Other
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177420042A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008564.9,