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rs587776664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAG;CAG) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs587776664(-;-)
Make rs587776664(-;TG)
ReferenceGRCh38 38.1/142
Chromosome3
Position57198399
GeneHESX1
is asnp
is mentioned by
dbSNPrs587776664
ebirs587776664
HLIrs587776664
Exacrs587776664
Varsomers587776664
Maprs587776664
PheGenIrs587776664
hapmaprs587776664
1000 genomesrs587776664
hgdprs587776664
ensemblrs587776664
gopubmedrs587776664
geneviewrs587776664
scholarrs587776664
googlers587776664
pharmgkbrs587776664
gwascentralrs587776664
openSNPrs587776664
23andMers587776664
23andMe allrs587776664
SNP Nexus

SNPshotrs587776664
SNPdbers587776664
MSV3drs587776664
GWAS Ctlgrs587776664
Max Magnitude0
ClinVar
Risk rs587776664(TGG,G;TGG,G)
Alt rs587776664(TGG,G;TGG,G)
Reference rs587776664(CAG;CAG)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene HESX1
CLNDBN Pituitary hormone deficiency, combined 5
Reversed 1
HGVS NC_000003.11:g.57232427_57232428delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000008136.3,