rs74315407
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs74315407(A;A) |
Make rs74315407(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 4699848 |
Gene | PRNP |
is a | snp |
is | mentioned by |
dbSNP | rs74315407 |
dbSNP (classic) | rs74315407 |
ClinGen | rs74315407 |
ebi | rs74315407 |
HLI | rs74315407 |
Exac | rs74315407 |
Gnomad | rs74315407 |
Varsome | rs74315407 |
LitVar | rs74315407 |
Map | rs74315407 |
PheGenI | rs74315407 |
Biobank | rs74315407 |
1000 genomes | rs74315407 |
hgdp | rs74315407 |
ensembl | rs74315407 |
geneview | rs74315407 |
scholar | rs74315407 |
rs74315407 | |
pharmgkb | rs74315407 |
gwascentral | rs74315407 |
openSNP | rs74315407 |
23andMe | rs74315407 |
SNPshot | rs74315407 |
SNPdbe | rs74315407 |
MSV3d | rs74315407 |
GWAS Ctlg | rs74315407 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74315407(A;A) |
Alt | rs74315407(A;A) |
Reference | Rs74315407(G;G) |
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.4680494G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000014342.21, RCV000020255.1, |
[PMID 7902693] A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.
[PMID 10526198] Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease.