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rs5748469

From SNPedia

Orientationplus
Stabilizedplus
Make rs5748469(A;A)
Make rs5748469(A;C)
Make rs5748469(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position19919576
GeneTXNRD2
is asnp
is mentioned by
dbSNPrs5748469
ebirs5748469
HLIrs5748469
Exacrs5748469
Varsomers5748469
Maprs5748469
PheGenIrs5748469
hapmaprs5748469
1000 genomesrs5748469
hgdprs5748469
ensemblrs5748469
gopubmedrs5748469
geneviewrs5748469
scholarrs5748469
googlers5748469
pharmgkbrs5748469
gwascentralrs5748469
openSNPrs5748469
23andMers5748469
23andMe allrs5748469
SNP Nexus

SNPshotrs5748469
SNPdbers5748469
MSV3drs5748469
GWAS Ctlgrs5748469
GMAF0.4894
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 20178852] Association Study between Polymorphisms in Selenoprotein Genes and Susceptibility to Kashin-Beck Disease


[PMID 17601350OA-icon.png] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.


GET Evidence
TXNRD2-A66S
aa_change Ala66Ser
aa_change_short A66S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.298376
summary



[PMID 24058403OA-icon.png] Association study of polymorphisms in selenoprotein genes and Kashin-Beck disease and serum selenium/iodine concentration in a Tibetan population