rs6107516
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6107516(A;A) |
Make rs6107516(A;G) |
Make rs6107516(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 4696446 |
Gene | PRNP |
is a | snp |
is | mentioned by |
dbSNP | rs6107516 |
dbSNP (classic) | rs6107516 |
ClinGen | rs6107516 |
ebi | rs6107516 |
HLI | rs6107516 |
Exac | rs6107516 |
Gnomad | rs6107516 |
Varsome | rs6107516 |
LitVar | rs6107516 |
Map | rs6107516 |
PheGenI | rs6107516 |
Biobank | rs6107516 |
1000 genomes | rs6107516 |
hgdp | rs6107516 |
ensembl | rs6107516 |
geneview | rs6107516 |
scholar | rs6107516 |
rs6107516 | |
pharmgkb | rs6107516 |
gwascentral | rs6107516 |
openSNP | rs6107516 |
23andMe | rs6107516 |
SNPshot | rs6107516 |
SNPdbe | rs6107516 |
MSV3d | rs6107516 |
GWAS Ctlg | rs6107516 |
GMAF | 0.1869 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22137330] |
Trait | |
Title | Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. |
Risk Allele | |
P-val | 3E-18 |
Odds Ratio | None None |
[PMID 19081515] Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.