rs11853426
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11853426(C;C) |
Make rs11853426(C;T) |
Make rs11853426(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 60317231 |
is a | snp |
is | mentioned by |
dbSNP | rs11853426 |
dbSNP (classic) | rs11853426 |
ClinGen | rs11853426 |
ebi | rs11853426 |
HLI | rs11853426 |
Exac | rs11853426 |
Gnomad | rs11853426 |
Varsome | rs11853426 |
LitVar | rs11853426 |
Map | rs11853426 |
PheGenI | rs11853426 |
Biobank | rs11853426 |
1000 genomes | rs11853426 |
hgdp | rs11853426 |
ensembl | rs11853426 |
geneview | rs11853426 |
scholar | rs11853426 |
rs11853426 | |
pharmgkb | rs11853426 |
gwascentral | rs11853426 |
openSNP | rs11853426 |
23andMe | rs11853426 |
SNPshot | rs11853426 |
SNPdbe | rs11853426 |
MSV3d | rs11853426 |
GWAS Ctlg | rs11853426 |
GMAF | 0.4518 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients