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rs9954153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 2 ~5x higher risk for Fuchs' dystrophy, a corneal disorder
(G;T) 2 ~2.5x higher risk for Fuchs' dystrophy, a corneal disorder
(T;T) 0 common
ReferenceGRCh38 38.1/141
Chromosome18
Position55871026
is asnp
is mentioned by
dbSNPrs9954153
ebirs9954153
HLIrs9954153
Exacrs9954153
Varsomers9954153
Maprs9954153
PheGenIrs9954153
hapmaprs9954153
1000 genomesrs9954153
hgdprs9954153
ensemblrs9954153
gopubmedrs9954153
geneviewrs9954153
scholarrs9954153
googlers9954153
pharmgkbrs9954153
gwascentralrs9954153
openSNPrs9954153
23andMers9954153
23andMe allrs9954153
SNP Nexus

SNPshotrs9954153
SNPdbers9954153
MSV3drs9954153
GWAS Ctlgrs9954153
GMAF0.1088
Max Magnitude2
rs9954153 is a SNP in the transcription factor 4 TCF4 gene. It is one of several TCF4 SNPs reported to be independently associated with Fuchs' dystrophy.
? (G;G) (G;T) (T;T) 28
[PMID 22234156OA-icon.png] Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process