rs41314453
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs41314453(C;T) |
Make rs41314453(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 133442704 |
Gene | ADAMTS13 |
is a | snp |
is | mentioned by |
dbSNP | rs41314453 |
dbSNP (classic) | rs41314453 |
ClinGen | rs41314453 |
ebi | rs41314453 |
HLI | rs41314453 |
Exac | rs41314453 |
Gnomad | rs41314453 |
Varsome | rs41314453 |
LitVar | rs41314453 |
Map | rs41314453 |
PheGenI | rs41314453 |
Biobank | rs41314453 |
1000 genomes | rs41314453 |
hgdp | rs41314453 |
ensembl | rs41314453 |
geneview | rs41314453 |
scholar | rs41314453 |
rs41314453 | |
pharmgkb | rs41314453 |
gwascentral | rs41314453 |
openSNP | rs41314453 |
23andMe | rs41314453 |
SNPshot | rs41314453 |
SNPdbe | rs41314453 |
MSV3d | rs41314453 |
GWAS Ctlg | rs41314453 |
Max Magnitude | 0 |
[PMID 25934476] Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity
ClinVar | |
---|---|
Risk | rs41314453(T;T) |
Alt | rs41314453(T;T) |
Reference | Rs41314453(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ADAMTS13 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.136307825C>T |
CLNSRC | |
CLNACC | RCV000220213.1, |