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rs587776681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGG;AGG) 0 common in clinvar
(CT;CT) 0 common in clinvar
Make rs587776681(-;-)
Make rs587776681(-;CT)
ReferenceGRCh38 38.1/142
Chromosome5
Position177994297
GenePROP1
is asnp
is mentioned by
dbSNPrs587776681
ebirs587776681
HLIrs587776681
Exacrs587776681
Varsomers587776681
Maprs587776681
PheGenIrs587776681
hapmaprs587776681
1000 genomesrs587776681
hgdprs587776681
ensemblrs587776681
gopubmedrs587776681
geneviewrs587776681
scholarrs587776681
googlers587776681
pharmgkbrs587776681
gwascentralrs587776681
openSNPrs587776681
23andMers587776681
23andMe allrs587776681
SNP Nexus

SNPshotrs587776681
SNPdbers587776681
MSV3drs587776681
GWAS Ctlgrs587776681
Max Magnitude0
ClinVar
Risk rs587776681(CTG,G;CTG,G)
Alt rs587776681(CTG,G;CTG,G)
Reference rs587776681(AGG;AGG)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421298_177421299delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000008565.3,