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rs587776712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776712(-;-)
Make rs587776712(-;A)
ReferenceGRCh38 38.1/142
Chromosome9
Position136200737
GeneLHX3
is asnp
is mentioned by
dbSNPrs587776712
ebirs587776712
HLIrs587776712
Exacrs587776712
Varsomers587776712
Maprs587776712
PheGenIrs587776712
hapmaprs587776712
1000 genomesrs587776712
hgdprs587776712
ensemblrs587776712
gopubmedrs587776712
geneviewrs587776712
scholarrs587776712
googlers587776712
pharmgkbrs587776712
gwascentralrs587776712
openSNPrs587776712
23andMers587776712
23andMe allrs587776712
SNP Nexus

SNPshotrs587776712
SNPdbers587776712
MSV3drs587776712
GWAS Ctlgrs587776712
Max Magnitude0
ClinVar
Risk rs587776712(;)
Alt rs587776712(;)
Reference rs587776712(A;A)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene LHX3
CLNDBN Pituitary hormone deficiency, combined 3
Reversed 0
HGVS NC_000009.11:g.139092583delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000009589.3,