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rs137854506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854506(A;T)
Make rs137854506(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136200700
GeneLHX3
is asnp
is mentioned by
dbSNPrs137854506
ebirs137854506
HLIrs137854506
Exacrs137854506
Varsomers137854506
Maprs137854506
PheGenIrs137854506
hapmaprs137854506
1000 genomesrs137854506
hgdprs137854506
ensemblrs137854506
gopubmedrs137854506
geneviewrs137854506
scholarrs137854506
googlers137854506
pharmgkbrs137854506
gwascentralrs137854506
openSNPrs137854506
23andMers137854506
23andMe allrs137854506
SNP Nexus

SNPshotrs137854506
SNPdbers137854506
MSV3drs137854506
GWAS Ctlgrs137854506
Max Magnitude0
OMIM600577
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137854506(T;T)
Alt rs137854506(T;T)
Reference rs137854506(A;A)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene LHX3
CLNDBN Pituitary hormone deficiency, combined 3
Reversed 1
HGVS NC_000009.11:g.139092546T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009595.2,