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rs6007897

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6007897(C;C)
Make rs6007897(C;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position46384624
GeneCELSR1
is asnp
is mentioned by
dbSNPrs6007897
ebirs6007897
HLIrs6007897
Exacrs6007897
Varsomers6007897
Maprs6007897
PheGenIrs6007897
hapmaprs6007897
1000 genomesrs6007897
hgdprs6007897
ensemblrs6007897
gopubmedrs6007897
geneviewrs6007897
scholarrs6007897
googlers6007897
pharmgkbrs6007897
gwascentralrs6007897
openSNPrs6007897
23andMers6007897
23andMe allrs6007897
SNP Nexus

SNPshotrs6007897
SNPdbers6007897
MSV3drs6007897
GWAS Ctlgrs6007897
GMAF0.2227
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19403135] Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study


[PMID 18454203OA-icon.png] Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.


GET Evidence
CELSR1-T2268A
aa_change Thr2268Ala
aa_change_short T2268A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.300985
summary



[PMID 26480662] [Association Between SNP rs6007897 of CELSR1 and Acute Ischemic Stroke in Western China Han Population: a Case-control Study]