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rs121912643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912643(G;G)
Make rs121912643(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position180271497
GeneLHX4
is asnp
is mentioned by
dbSNPrs121912643
ebirs121912643
HLIrs121912643
Exacrs121912643
Varsomers121912643
Maprs121912643
PheGenIrs121912643
hapmaprs121912643
1000 genomesrs121912643
hgdprs121912643
ensemblrs121912643
gopubmedrs121912643
geneviewrs121912643
scholarrs121912643
googlers121912643
pharmgkbrs121912643
gwascentralrs121912643
openSNPrs121912643
23andMers121912643
23andMe allrs121912643
SNP Nexus

SNPshotrs121912643
SNPdbers121912643
MSV3drs121912643
GWAS Ctlgrs121912643
Max Magnitude0
OMIM602146
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912643(G;G)
Alt rs121912643(G;G)
Reference rs121912643(T;T)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene LHX4 LHX4-AS1
CLNDBN Pituitary hormone deficiency, combined 4
Reversed 0
HGVS NC_000001.10:g.180240632T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000007938.3,