rs730566
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs730566(G;G) |
Make rs730566(G;T) |
Make rs730566(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 48445644 |
Gene | ATRIP, CCDC51 |
is a | snp |
is | mentioned by |
dbSNP | rs730566 |
dbSNP (classic) | rs730566 |
ClinGen | rs730566 |
ebi | rs730566 |
HLI | rs730566 |
Exac | rs730566 |
Gnomad | rs730566 |
Varsome | rs730566 |
LitVar | rs730566 |
Map | rs730566 |
PheGenI | rs730566 |
Biobank | rs730566 |
1000 genomes | rs730566 |
hgdp | rs730566 |
ensembl | rs730566 |
geneview | rs730566 |
scholar | rs730566 |
rs730566 | |
pharmgkb | rs730566 |
gwascentral | rs730566 |
openSNP | rs730566 |
23andMe | rs730566 |
SNPshot | rs730566 |
SNPdbe | rs730566 |
MSV3d | rs730566 |
GWAS Ctlg | rs730566 |
GMAF | 0.3384 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22210626] |
Trait | |
Title | Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. |
Risk Allele | |
P-val | 0.000007 |
Odds Ratio | 1.2700 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d