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rs786204780

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204780(A;C)
Make rs786204780(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position180271378
GeneLHX4, LHX4-AS1
is asnp
is mentioned by
dbSNPrs786204780
ebirs786204780
HLIrs786204780
Exacrs786204780
Varsomers786204780
Maprs786204780
PheGenIrs786204780
hapmaprs786204780
1000 genomesrs786204780
hgdprs786204780
ensemblrs786204780
gopubmedrs786204780
geneviewrs786204780
scholarrs786204780
googlers786204780
pharmgkbrs786204780
gwascentralrs786204780
openSNPrs786204780
23andMers786204780
23andMe allrs786204780
SNP Nexus

SNPshotrs786204780
SNPdbers786204780
MSV3drs786204780
GWAS Ctlgrs786204780
Max Magnitude0
ClinVar
Risk rs786204780(C;C)
Alt rs786204780(C;C)
Reference rs786204780(A;A)
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.180240513A>C
CLNSRC
CLNACC RCV000169664.1,