rs1970546
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1970546(A;A) |
Make rs1970546(A;G) |
Make rs1970546(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 61278882 |
Gene | CDH4 |
is a | snp |
is | mentioned by |
dbSNP | rs1970546 |
dbSNP (classic) | rs1970546 |
ClinGen | rs1970546 |
ebi | rs1970546 |
HLI | rs1970546 |
Exac | rs1970546 |
Gnomad | rs1970546 |
Varsome | rs1970546 |
LitVar | rs1970546 |
Map | rs1970546 |
PheGenI | rs1970546 |
Biobank | rs1970546 |
1000 genomes | rs1970546 |
hgdp | rs1970546 |
ensembl | rs1970546 |
geneview | rs1970546 |
scholar | rs1970546 |
rs1970546 | |
pharmgkb | rs1970546 |
gwascentral | rs1970546 |
openSNP | rs1970546 |
23andMe | rs1970546 |
SNPshot | rs1970546 |
SNPdbe | rs1970546 |
MSV3d | rs1970546 |
GWAS Ctlg | rs1970546 |
GMAF | 0.275 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs1970546 |
PubMedID | [PMID 17903297] |
Condition | Volumetric brain MRI |
Gene | CDH4 |
Risk Allele | |
pValue | 4.00E-008 |
OR | NA |
95% CI |
[PMID 17903291] The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.