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rs587776683

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776683(-;-)
Make rs587776683(-;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position177994298
GenePROP1
is asnp
is mentioned by
dbSNPrs587776683
ebirs587776683
HLIrs587776683
Exacrs587776683
Varsomers587776683
Maprs587776683
PheGenIrs587776683
hapmaprs587776683
1000 genomesrs587776683
hgdprs587776683
ensemblrs587776683
gopubmedrs587776683
geneviewrs587776683
scholarrs587776683
googlers587776683
pharmgkbrs587776683
gwascentralrs587776683
openSNPrs587776683
23andMers587776683
23andMe allrs587776683
SNP Nexus

SNPshotrs587776683
SNPdbers587776683
MSV3drs587776683
GWAS Ctlgrs587776683
Max Magnitude0
ClinVar
Risk rs587776683(;)
Alt rs587776683(;)
Reference rs587776683(T;T)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 0
HGVS NC_000005.9:g.177421299delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008570.4,