rs2275697
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2275697(C;C) |
Make rs2275697(C;T) |
Make rs2275697(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 205058609 |
Gene | CNTN2 |
is a | snp |
is | mentioned by |
dbSNP | rs2275697 |
dbSNP (classic) | rs2275697 |
ClinGen | rs2275697 |
ebi | rs2275697 |
HLI | rs2275697 |
Exac | rs2275697 |
Gnomad | rs2275697 |
Varsome | rs2275697 |
LitVar | rs2275697 |
Map | rs2275697 |
PheGenI | rs2275697 |
Biobank | rs2275697 |
1000 genomes | rs2275697 |
hgdp | rs2275697 |
ensembl | rs2275697 |
geneview | rs2275697 |
scholar | rs2275697 |
rs2275697 | |
pharmgkb | rs2275697 |
gwascentral | rs2275697 |
openSNP | rs2275697 |
23andMe | rs2275697 |
SNPshot | rs2275697 |
SNPdbe | rs2275697 |
MSV3d | rs2275697 |
GWAS Ctlg | rs2275697 |
GMAF | 0.2314 |
Max Magnitude | 0 |
? | (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