rs7199949
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7199949(C;C) |
Make rs7199949(C;G) |
Make rs7199949(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 31084843 |
Gene | PRSS53 |
is a | snp |
is | mentioned by |
dbSNP | rs7199949 |
dbSNP (classic) | rs7199949 |
ClinGen | rs7199949 |
ebi | rs7199949 |
HLI | rs7199949 |
Exac | rs7199949 |
Gnomad | rs7199949 |
Varsome | rs7199949 |
LitVar | rs7199949 |
Map | rs7199949 |
PheGenI | rs7199949 |
Biobank | rs7199949 |
1000 genomes | rs7199949 |
hgdp | rs7199949 |
ensembl | rs7199949 |
geneview | rs7199949 |
scholar | rs7199949 |
rs7199949 | |
pharmgkb | rs7199949 |
gwascentral | rs7199949 |
openSNP | rs7199949 |
23andMe | rs7199949 |
SNPshot | rs7199949 |
SNPdbe | rs7199949 |
MSV3d | rs7199949 |
GWAS Ctlg | rs7199949 |
GMAF | 0.3526 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 21590310] Evaluation of the effects of VKORC1 polymorphisms and haplotypes, CYP2C9 genotypes, and clinical factors on warfarin response in Sudanese patients