rs397515437
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs397515437(A;A) |
Make rs397515437(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 83542270 |
Gene | VCAN, VCAN-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs397515437 |
dbSNP (classic) | rs397515437 |
ClinGen | rs397515437 |
ebi | rs397515437 |
HLI | rs397515437 |
Exac | rs397515437 |
Gnomad | rs397515437 |
Varsome | rs397515437 |
LitVar | rs397515437 |
Map | rs397515437 |
PheGenI | rs397515437 |
Biobank | rs397515437 |
1000 genomes | rs397515437 |
hgdp | rs397515437 |
ensembl | rs397515437 |
geneview | rs397515437 |
scholar | rs397515437 |
rs397515437 | |
pharmgkb | rs397515437 |
gwascentral | rs397515437 |
openSNP | rs397515437 |
23andMe | rs397515437 |
SNPshot | rs397515437 |
SNPdbe | rs397515437 |
MSV3d | rs397515437 |
GWAS Ctlg | rs397515437 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397515437(A;A) |
Alt | rs397515437(A;A) |
Reference | Rs397515437(T;T) |
Significance | Pathogenic |
Disease | Wagner syndrome |
Variation | info |
Gene | LOC105379054 VCAN |
CLNDBN | Wagner syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.82838089T>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000034808.30, |