rs864309744
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs864309744(A;A) |
Make rs864309744(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 83537001 |
Gene | VCAN, VCAN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs864309744 |
dbSNP (classic) | rs864309744 |
ClinGen | rs864309744 |
ebi | rs864309744 |
HLI | rs864309744 |
Exac | rs864309744 |
Gnomad | rs864309744 |
Varsome | rs864309744 |
LitVar | rs864309744 |
Map | rs864309744 |
PheGenI | rs864309744 |
Biobank | rs864309744 |
1000 genomes | rs864309744 |
hgdp | rs864309744 |
ensembl | rs864309744 |
geneview | rs864309744 |
scholar | rs864309744 |
rs864309744 | |
pharmgkb | rs864309744 |
gwascentral | rs864309744 |
openSNP | rs864309744 |
23andMe | rs864309744 |
SNPshot | rs864309744 |
SNPdbe | rs864309744 |
MSV3d | rs864309744 |
GWAS Ctlg | rs864309744 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864309744(A;A) |
Alt | rs864309744(A;A) |
Reference | Rs864309744(T;T) |
Significance | Pathogenic |
Disease | Wagner syndrome |
Variation | info |
Gene | LOC105379054 VCAN |
CLNDBN | Wagner syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.82832820T>A |
CLNSRC | |
CLNACC | RCV000203372.1, |