rs1727638
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1727638(A;A) |
Make rs1727638(A;G) |
Make rs1727638(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 71429869 |
Gene | LINC01626 |
is a | snp |
is | mentioned by |
dbSNP | rs1727638 |
dbSNP (classic) | rs1727638 |
ClinGen | rs1727638 |
ebi | rs1727638 |
HLI | rs1727638 |
Exac | rs1727638 |
Gnomad | rs1727638 |
Varsome | rs1727638 |
LitVar | rs1727638 |
Map | rs1727638 |
PheGenI | rs1727638 |
Biobank | rs1727638 |
1000 genomes | rs1727638 |
hgdp | rs1727638 |
ensembl | rs1727638 |
geneview | rs1727638 |
scholar | rs1727638 |
rs1727638 | |
pharmgkb | rs1727638 |
gwascentral | rs1727638 |
openSNP | rs1727638 |
23andMe | rs1727638 |
SNPshot | rs1727638 |
SNPdbe | rs1727638 |
MSV3d | rs1727638 |
GWAS Ctlg | rs1727638 |
GMAF | 0.4545 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 0.000001 |
Odds Ratio | None None |