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rs2275697

From SNPedia

Orientationminus
Stabilizedminus
Make rs2275697(C;C)
Make rs2275697(C;T)
Make rs2275697(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position205058609
GeneCNTN2
is asnp
is mentioned by
dbSNPrs2275697
ebirs2275697
HLIrs2275697
Exacrs2275697
Varsomers2275697
Maprs2275697
PheGenIrs2275697
hapmaprs2275697
1000 genomesrs2275697
hgdprs2275697
ensemblrs2275697
gopubmedrs2275697
geneviewrs2275697
scholarrs2275697
googlers2275697
pharmgkbrs2275697
gwascentralrs2275697
openSNPrs2275697
23andMers2275697
23andMe allrs2275697
SNP Nexus

SNPshotrs2275697
SNPdbers2275697
MSV3drs2275697
GWAS Ctlgrs2275697
GMAF0.2314
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 22462668] Single-nucleotide polymorphism of transient axonal glycoprotein-1 and its correlation with clinical features and prognosis in chronic inflammatory demyelinating polyneuropathy


GET Evidence
CNTN2-A145T
aa_change Ala145Thr
aa_change_short A145T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.152909
summary