rs1031261
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1031261(C;C) |
Make rs1031261(C;G) |
Make rs1031261(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 32640454 |
Gene | TTC27 |
is a | snp |
is | mentioned by |
dbSNP | rs1031261 |
dbSNP (classic) | rs1031261 |
ClinGen | rs1031261 |
ebi | rs1031261 |
HLI | rs1031261 |
Exac | rs1031261 |
Gnomad | rs1031261 |
Varsome | rs1031261 |
LitVar | rs1031261 |
Map | rs1031261 |
PheGenI | rs1031261 |
Biobank | rs1031261 |
1000 genomes | rs1031261 |
hgdp | rs1031261 |
ensembl | rs1031261 |
geneview | rs1031261 |
scholar | rs1031261 |
rs1031261 | |
pharmgkb | rs1031261 |
gwascentral | rs1031261 |
openSNP | rs1031261 |
23andMe | rs1031261 |
SNPshot | rs1031261 |
SNPdbe | rs1031261 |
MSV3d | rs1031261 |
GWAS Ctlg | rs1031261 |
GMAF | 0.1635 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22745009] |
Trait | |
Title | Multiple loci influencing hippocampal degeneration identified by genome scan. |
Risk Allele | C |
P-val | 0.000002 |
Odds Ratio | None None |