rs2317676
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2317676(A;G) |
Make rs2317676(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 47310917 |
Gene | ITGB3, THCAT158 |
is a | snp |
is | mentioned by |
dbSNP | rs2317676 |
dbSNP (classic) | rs2317676 |
ClinGen | rs2317676 |
ebi | rs2317676 |
HLI | rs2317676 |
Exac | rs2317676 |
Gnomad | rs2317676 |
Varsome | rs2317676 |
LitVar | rs2317676 |
Map | rs2317676 |
PheGenI | rs2317676 |
Biobank | rs2317676 |
1000 genomes | rs2317676 |
hgdp | rs2317676 |
ensembl | rs2317676 |
geneview | rs2317676 |
scholar | rs2317676 |
rs2317676 | |
pharmgkb | rs2317676 |
gwascentral | rs2317676 |
openSNP | rs2317676 |
23andMe | rs2317676 |
SNPshot | rs2317676 |
SNPdbe | rs2317676 |
MSV3d | rs2317676 |
GWAS Ctlg | rs2317676 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24777809] SNPs in MicroRNA-Binding Sites in the ITGB1 and ITGB3 3'-UTR Increase Colorectal Cancer Risk
ClinVar | |
---|---|
Risk | rs2317676(G;G) |
Alt | rs2317676(G;G) |
Reference | Rs2317676(A;A) |
Significance | Probable-non-pathogenic |
Disease | Glanzmann thrombasthenia |
Variation | info |
Gene | ITGB3 THCAT158 |
CLNDBN | Glanzmann thrombasthenia |
Reversed | 0 |
HGVS | NC_000017.10:g.45388283A>G |
CLNSRC | |
CLNACC | RCV000310133.1, |