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rs121912644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912644(A;A)
Make rs121912644(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position180274568
GeneLHX4
is asnp
is mentioned by
dbSNPrs121912644
ebirs121912644
HLIrs121912644
Exacrs121912644
Varsomers121912644
Maprs121912644
PheGenIrs121912644
hapmaprs121912644
1000 genomesrs121912644
hgdprs121912644
ensemblrs121912644
gopubmedrs121912644
geneviewrs121912644
scholarrs121912644
googlers121912644
pharmgkbrs121912644
gwascentralrs121912644
openSNPrs121912644
23andMers121912644
23andMe allrs121912644
SNP Nexus

SNPshotrs121912644
SNPdbers121912644
MSV3drs121912644
GWAS Ctlgrs121912644
Max Magnitude0
OMIM602146
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121912644(A;A)
Alt rs121912644(A;A)
Reference rs121912644(C;C)
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.180243703C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007939.2,