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rs794726693

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794726693(C;T)
Make rs794726693(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177994174
GenePROP1
is asnp
is mentioned by
dbSNPrs794726693
ebirs794726693
HLIrs794726693
Exacrs794726693
Varsomers794726693
Maprs794726693
PheGenIrs794726693
hapmaprs794726693
1000 genomesrs794726693
hgdprs794726693
ensemblrs794726693
gopubmedrs794726693
geneviewrs794726693
scholarrs794726693
googlers794726693
pharmgkbrs794726693
gwascentralrs794726693
openSNPrs794726693
23andMers794726693
23andMe allrs794726693
SNP Nexus

SNPshotrs794726693
SNPdbers794726693
MSV3drs794726693
GWAS Ctlgrs794726693
Max Magnitude0
ClinVar
Risk rs794726693(T;T)
Alt rs794726693(T;T)
Reference rs794726693(C;C)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421175G>A
CLNSRC
CLNACC RCV000148938.2,