rs74315409
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs74315409(G;G) |
Make rs74315409(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 4699915 |
Gene | PRNP |
is a | snp |
is | mentioned by |
dbSNP | rs74315409 |
dbSNP (classic) | rs74315409 |
ClinGen | rs74315409 |
ebi | rs74315409 |
HLI | rs74315409 |
Exac | rs74315409 |
Gnomad | rs74315409 |
Varsome | rs74315409 |
LitVar | rs74315409 |
Map | rs74315409 |
PheGenI | rs74315409 |
Biobank | rs74315409 |
1000 genomes | rs74315409 |
hgdp | rs74315409 |
ensembl | rs74315409 |
geneview | rs74315409 |
scholar | rs74315409 |
rs74315409 | |
pharmgkb | rs74315409 |
gwascentral | rs74315409 |
openSNP | rs74315409 |
23andMe | rs74315409 |
SNPshot | rs74315409 |
SNPdbe | rs74315409 |
MSV3d | rs74315409 |
GWAS Ctlg | rs74315409 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74315409(G;G) |
Alt | rs74315409(G;G) |
Reference | Rs74315409(T;T) |
Significance | Pathogenic |
Disease | Jakob-Creutzfeldt disease Genetic prion diseases |
Variation | info |
Gene | PRNP |
CLNDBN | Jakob-Creutzfeldt disease Genetic prion diseases |
Reversed | 0 |
HGVS | NC_000020.10:g.4680561T>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000014345.13, RCV000020258.1, |
[PMID 8461023] Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome.