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rs137854505

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137854505(A;A)
Make rs137854505(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position136198755
GeneLHX3
is asnp
is mentioned by
dbSNPrs137854505
ebirs137854505
HLIrs137854505
Exacrs137854505
Varsomers137854505
Maprs137854505
PheGenIrs137854505
hapmaprs137854505
1000 genomesrs137854505
hgdprs137854505
ensemblrs137854505
gopubmedrs137854505
geneviewrs137854505
scholarrs137854505
googlers137854505
pharmgkbrs137854505
gwascentralrs137854505
openSNPrs137854505
23andMers137854505
23andMe allrs137854505
SNP Nexus

SNPshotrs137854505
SNPdbers137854505
MSV3drs137854505
GWAS Ctlgrs137854505
Max Magnitude0
OMIM600577
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137854505(A;A)
Alt rs137854505(A;A)
Reference rs137854505(G;G)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene LHX3
CLNDBN Pituitary hormone deficiency, combined 3
Reversed 1
HGVS NC_000009.11:g.139090601C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009593.5,