rs1800380
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 6029429 |
Gene | VWF |
is a | snp |
is | mentioned by |
dbSNP | rs1800380 |
dbSNP (classic) | rs1800380 |
ClinGen | rs1800380 |
ebi | rs1800380 |
HLI | rs1800380 |
Exac | rs1800380 |
Gnomad | rs1800380 |
Varsome | rs1800380 |
LitVar | rs1800380 |
Map | rs1800380 |
PheGenI | rs1800380 |
Biobank | rs1800380 |
1000 genomes | rs1800380 |
hgdp | rs1800380 |
ensembl | rs1800380 |
geneview | rs1800380 |
scholar | rs1800380 |
rs1800380 | |
pharmgkb | rs1800380 |
gwascentral | rs1800380 |
openSNP | rs1800380 |
23andMe | rs1800380 |
SNPshot | rs1800380 |
SNPdbe | rs1800380 |
MSV3d | rs1800380 |
GWAS Ctlg | rs1800380 |
Max Magnitude | 0 |
[PMID 25779970] Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans
ClinVar | |
---|---|
Risk | rs1800380(A;A) |
Alt | rs1800380(A;A) |
Reference | Rs1800380(G;G) |
Significance | Probable-non-pathogenic |
Disease | not specified von Willebrand disorder |
Variation | info |
Gene | VWF |
CLNDBN | not specified von Willebrand disorder |
Reversed | 1 |
HGVS | NC_000012.11:g.6138595C>T |
CLNSRC | |
CLNACC | RCV000176272.2, RCV000314525.1, |