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rs17595731

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 2.5 ~20-30x higher risk for Fuchs' dystrophy, a corneal disorder
(C;G) 2.5 ~5 fold higher risk for Fuchs' dystrophy, a corneal disorder
(G;G) 0 common
ReferenceGRCh38 38.1/141
Chromosome18
Position55440221
GeneTCF4
is asnp
is mentioned by
dbSNPrs17595731
ebirs17595731
HLIrs17595731
Exacrs17595731
Varsomers17595731
Maprs17595731
PheGenIrs17595731
hapmaprs17595731
1000 genomesrs17595731
hgdprs17595731
ensemblrs17595731
gopubmedrs17595731
geneviewrs17595731
scholarrs17595731
googlers17595731
pharmgkbrs17595731
gwascentralrs17595731
openSNPrs17595731
23andMers17595731
23andMe allrs17595731
SNP Nexus

SNPshotrs17595731
SNPdbers17595731
MSV3drs17595731
GWAS Ctlgrs17595731
GMAF0.04545
Max Magnitude2.5
rs17595731 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.
? (C;C) (C;G) (G;G) 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