rs886054846
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AGA;AGA) | 0 | common in clinvar |
Chromosome | 2 |
Position | 127426126 |
Gene | LOC105373608, PROC |
is a | snp |
is | mentioned by |
dbSNP | rs886054846 |
dbSNP (classic) | rs886054846 |
ClinGen | rs886054846 |
ebi | rs886054846 |
HLI | rs886054846 |
Exac | rs886054846 |
Gnomad | rs886054846 |
Varsome | rs886054846 |
LitVar | rs886054846 |
Map | rs886054846 |
PheGenI | rs886054846 |
Biobank | rs886054846 |
1000 genomes | rs886054846 |
hgdp | rs886054846 |
ensembl | rs886054846 |
geneview | rs886054846 |
scholar | rs886054846 |
rs886054846 | |
pharmgkb | rs886054846 |
gwascentral | rs886054846 |
openSNP | rs886054846 |
23andMe | rs886054846 |
SNPshot | rs886054846 |
SNPdbe | rs886054846 |
MSV3d | rs886054846 |
GWAS Ctlg | rs886054846 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886054846(-;-) |
Alt | rs886054846(-;-) |
Reference | Rs886054846(AGA;AGA) |
Significance | Other |
Disease | Thrombophilia |
Variation | info |
Gene | PROC |
CLNDBN | Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant |
Reversed | 0 |
HGVS | NC_000002.11:g.128183702_128183704delAAG |
CLNSRC | Illumina |
CLNACC | RCV000288890.1, |