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rs2229569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2229569(C;T)
Make rs2229569(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169704697
GeneSELL
is asnp
is mentioned by
dbSNPrs2229569
ebirs2229569
HLIrs2229569
Exacrs2229569
Varsomers2229569
Maprs2229569
PheGenIrs2229569
hapmaprs2229569
1000 genomesrs2229569
hgdprs2229569
ensemblrs2229569
gopubmedrs2229569
geneviewrs2229569
scholarrs2229569
googlers2229569
pharmgkbrs2229569
gwascentralrs2229569
openSNPrs2229569
23andMers2229569
23andMe allrs2229569
SNP Nexus

SNPshotrs2229569
SNPdbers2229569
MSV3drs2229569
GWAS Ctlgrs2229569
Merged fromRs4987310
GMAF0.2397
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19064790OA-icon.png] Predictive genomics of cardioembolic stroke.


[PMID 19240957] Candidate gene analysis of selectin cluster in patients with multiple sclerosis.

GET Evidence
SELL-P213S
aa_change Pro213Ser
aa_change_short P213S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.156902
summary



[PMID 22646485OA-icon.png] Association between genetic variants in adhesion molecules and outcomes after hematopoietic cell transplants