rs2935776
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2935776(C;C) |
Make rs2935776(C;T) |
Make rs2935776(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 108617674 |
Gene | TMEM74 |
is a | snp |
is | mentioned by |
dbSNP | rs2935776 |
dbSNP (classic) | rs2935776 |
ClinGen | rs2935776 |
ebi | rs2935776 |
HLI | rs2935776 |
Exac | rs2935776 |
Gnomad | rs2935776 |
Varsome | rs2935776 |
LitVar | rs2935776 |
Map | rs2935776 |
PheGenI | rs2935776 |
Biobank | rs2935776 |
1000 genomes | rs2935776 |
hgdp | rs2935776 |
ensembl | rs2935776 |
geneview | rs2935776 |
scholar | rs2935776 |
rs2935776 | |
pharmgkb | rs2935776 |
gwascentral | rs2935776 |
openSNP | rs2935776 |
23andMe | rs2935776 |
SNPshot | rs2935776 |
SNPdbe | rs2935776 |
MSV3d | rs2935776 |
GWAS Ctlg | rs2935776 |
GMAF | 0.2424 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 6E-7 |
Odds Ratio | None None |