rs1943816
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs1943816(C;C) |
Make rs1943816(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 73391387 |
is a | snp |
is | mentioned by |
dbSNP | rs1943816 |
dbSNP (classic) | rs1943816 |
ClinGen | rs1943816 |
ebi | rs1943816 |
HLI | rs1943816 |
Exac | rs1943816 |
Gnomad | rs1943816 |
Varsome | rs1943816 |
LitVar | rs1943816 |
Map | rs1943816 |
PheGenI | rs1943816 |
Biobank | rs1943816 |
1000 genomes | rs1943816 |
hgdp | rs1943816 |
ensembl | rs1943816 |
geneview | rs1943816 |
scholar | rs1943816 |
rs1943816 | |
pharmgkb | rs1943816 |
gwascentral | rs1943816 |
openSNP | rs1943816 |
23andMe | rs1943816 |
SNPshot | rs1943816 |
SNPdbe | rs1943816 |
MSV3d | rs1943816 |
GWAS Ctlg | rs1943816 |
GMAF | 0.1942 |
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 | 1E-7 |
Odds Ratio | None None |