rs6599001
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6599001(C;C) |
Make rs6599001(C;T) |
Make rs6599001(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 39032660 |
Gene | SCN11A |
is a | snp |
is | mentioned by |
dbSNP | rs6599001 |
dbSNP (classic) | rs6599001 |
ClinGen | rs6599001 |
ebi | rs6599001 |
HLI | rs6599001 |
Exac | rs6599001 |
Gnomad | rs6599001 |
Varsome | rs6599001 |
LitVar | rs6599001 |
Map | rs6599001 |
PheGenI | rs6599001 |
Biobank | rs6599001 |
1000 genomes | rs6599001 |
hgdp | rs6599001 |
ensembl | rs6599001 |
geneview | rs6599001 |
scholar | rs6599001 |
rs6599001 | |
pharmgkb | rs6599001 |
gwascentral | rs6599001 |
openSNP | rs6599001 |
23andMe | rs6599001 |
SNPshot | rs6599001 |
SNPdbe | rs6599001 |
MSV3d | rs6599001 |
GWAS Ctlg | rs6599001 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26186006] Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal