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rs121909173

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909173(C;C)
Make rs121909173(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position57199901
GeneHESX1
is asnp
is mentioned by
dbSNPrs121909173
ebirs121909173
HLIrs121909173
Exacrs121909173
Varsomers121909173
Maprs121909173
PheGenIrs121909173
hapmaprs121909173
1000 genomesrs121909173
hgdprs121909173
ensemblrs121909173
gopubmedrs121909173
geneviewrs121909173
scholarrs121909173
googlers121909173
pharmgkbrs121909173
gwascentralrs121909173
openSNPrs121909173
23andMers121909173
23andMe allrs121909173
SNP Nexus

SNPshotrs121909173
SNPdbers121909173
MSV3drs121909173
GWAS Ctlgrs121909173
Max Magnitude0
OMIM601802
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121909173(C;C)
Alt rs121909173(C;C)
Reference rs121909173(G;G)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene HESX1
CLNDBN Pituitary hormone deficiency, combined 5
Reversed 1
HGVS NC_000003.11:g.57233929C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008139.4,