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rs794726694

From SNPedia
Merged intors587776682
Orientationminus
Stabilizedminus
Geno Mag Summary
(TCGAGTGCTCCAC;TCGAGTGCTCCAC) 0 common in clinvar
Make rs794726694(-;-)
Make rs794726694(-;ACTCGAGTGCTCC)
Make rs794726694(ACTCGAGTGCTCC;ACTCGAGTGCTCC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177994326
GenePROP1
is asnp
is mentioned by
dbSNPrs794726694
dbSNP (old)rs794726694
ClinGenrs794726694
ebirs794726694
HLIrs794726694
Exacrs794726694
Gnomadrs794726694
Varsomers794726694
Maprs794726694
PheGenIrs794726694
Biobankrs794726694
1000 genomesrs794726694
hgdprs794726694
ensemblrs794726694
gopubmedrs794726694
geneviewrs794726694
scholarrs794726694
googlers794726694
pharmgkbrs794726694
gwascentralrs794726694
openSNPrs794726694
23andMers794726694
23andMe allrs794726694
SNP Nexus

SNPshotrs794726694
SNPdbers794726694
MSV3drs794726694
GWAS Ctlgrs794726694
StatusMerged into rs587776682
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs794726694(TCGAGTGCTCCAC;TCGAGTGCTCCAC)
Significance Other
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421325_177421337delGTGGAGCACTCGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008569.3,