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rs17089887

From SNPedia

Orientationplus
Stabilizedplus
Make rs17089887(C;C)
Make rs17089887(C;T)
Make rs17089887(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position55541025
GeneTCF4
is asnp
is mentioned by
dbSNPrs17089887
ebirs17089887
HLIrs17089887
Exacrs17089887
Varsomers17089887
Maprs17089887
PheGenIrs17089887
hapmaprs17089887
1000 genomesrs17089887
hgdprs17089887
ensemblrs17089887
gopubmedrs17089887
geneviewrs17089887
scholarrs17089887
googlers17089887
pharmgkbrs17089887
gwascentralrs17089887
openSNPrs17089887
23andMers17089887
23andMe allrs17089887
SNP Nexus

SNPshotrs17089887
SNPdbers17089887
MSV3drs17089887
GWAS Ctlgrs17089887
GMAF0.1556
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21659310] Association of TCF4 Gene Polymorphisms with Fuchs Corneal Dystrophy in the Chinese