rs1997111
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1997111(G;G) |
Make rs1997111(G;T) |
Make rs1997111(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 118950113 |
Gene | LOC105370020 |
is a | snp |
is | mentioned by |
dbSNP | rs1997111 |
dbSNP (classic) | rs1997111 |
ClinGen | rs1997111 |
ebi | rs1997111 |
HLI | rs1997111 |
Exac | rs1997111 |
Gnomad | rs1997111 |
Varsome | rs1997111 |
LitVar | rs1997111 |
Map | rs1997111 |
PheGenI | rs1997111 |
Biobank | rs1997111 |
1000 genomes | rs1997111 |
hgdp | rs1997111 |
ensembl | rs1997111 |
geneview | rs1997111 |
scholar | rs1997111 |
rs1997111 | |
pharmgkb | rs1997111 |
gwascentral | rs1997111 |
openSNP | rs1997111 |
23andMe | rs1997111 |
SNPshot | rs1997111 |
SNPdbe | rs1997111 |
MSV3d | rs1997111 |
GWAS Ctlg | rs1997111 |
GMAF | 0.3774 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20932310] |
Trait | |
Title | Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study |
Risk Allele | T |
P-val | 1E-8 |
Odds Ratio | None None |