rs1006973
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1006973(A;A) |
Make rs1006973(A;G) |
Make rs1006973(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 51610371 |
Gene | FRMD6 |
is a | snp |
is | mentioned by |
dbSNP | rs1006973 |
dbSNP (classic) | rs1006973 |
ClinGen | rs1006973 |
ebi | rs1006973 |
HLI | rs1006973 |
Exac | rs1006973 |
Gnomad | rs1006973 |
Varsome | rs1006973 |
LitVar | rs1006973 |
Map | rs1006973 |
PheGenI | rs1006973 |
Biobank | rs1006973 |
1000 genomes | rs1006973 |
hgdp | rs1006973 |
ensembl | rs1006973 |
geneview | rs1006973 |
scholar | rs1006973 |
rs1006973 | |
pharmgkb | rs1006973 |
gwascentral | rs1006973 |
openSNP | rs1006973 |
23andMe | rs1006973 |
SNPshot | rs1006973 |
SNPdbe | rs1006973 |
MSV3d | rs1006973 |
GWAS Ctlg | rs1006973 |
GMAF | 0.3352 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22216198] |
Trait | |
Title | A genome-wide association study of the Protein C anticoagulant pathway. |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | None None |