rs5017717
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs5017717(C;T) |
Make rs5017717(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 93884869 |
Gene | PROS1 |
is a | snp |
is | mentioned by |
dbSNP | rs5017717 |
dbSNP (classic) | rs5017717 |
ClinGen | rs5017717 |
ebi | rs5017717 |
HLI | rs5017717 |
Exac | rs5017717 |
Gnomad | rs5017717 |
Varsome | rs5017717 |
LitVar | rs5017717 |
Map | rs5017717 |
PheGenI | rs5017717 |
Biobank | rs5017717 |
1000 genomes | rs5017717 |
hgdp | rs5017717 |
ensembl | rs5017717 |
geneview | rs5017717 |
scholar | rs5017717 |
rs5017717 | |
pharmgkb | rs5017717 |
gwascentral | rs5017717 |
openSNP | rs5017717 |
23andMe | rs5017717 |
SNPshot | rs5017717 |
SNPdbe | rs5017717 |
MSV3d | rs5017717 |
GWAS Ctlg | rs5017717 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs5017717(T;T) |
Alt | rs5017717(T;T) |
Reference | Rs5017717(C;C) |
Significance | Untested |
Disease | |
Variation | info |
Gene | PROS1 |
CLNDBN | OMIM |
Reversed | 1 |
HGVS | NC_000003.11:g.93603713G>A |
CLNSRC | |
CLNACC |