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rs587776662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776662(-;-)
Make rs587776662(-;C)
Make rs587776662(C;C)
ReferenceGRCh38 38.1/142
Chromosome1
Position180266436
GeneLHX4
is asnp
is mentioned by
dbSNPrs587776662
ebirs587776662
HLIrs587776662
Exacrs587776662
Varsomers587776662
Maprs587776662
PheGenIrs587776662
hapmaprs587776662
1000 genomesrs587776662
hgdprs587776662
ensemblrs587776662
gopubmedrs587776662
geneviewrs587776662
scholarrs587776662
googlers587776662
pharmgkbrs587776662
gwascentralrs587776662
openSNPrs587776662
23andMers587776662
23andMe allrs587776662
SNP Nexus

SNPshotrs587776662
SNPdbers587776662
MSV3drs587776662
GWAS Ctlgrs587776662
Max Magnitude0
ClinVar
Risk rs587776662(C;C)
Alt rs587776662(C;C)
Reference rs587776662(;)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene LHX4
CLNDBN Pituitary hormone deficiency, combined 4
Reversed 0
HGVS NC_000001.10:g.180235571dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007940.3,