rs488087
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs488087(C;T) |
Make rs488087(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 133071212 |
Gene | CEL |
is a | snp |
is | mentioned by |
dbSNP | rs488087 |
dbSNP (classic) | rs488087 |
ClinGen | rs488087 |
ebi | rs488087 |
HLI | rs488087 |
Exac | rs488087 |
Gnomad | rs488087 |
Varsome | rs488087 |
LitVar | rs488087 |
Map | rs488087 |
PheGenI | rs488087 |
Biobank | rs488087 |
1000 genomes | rs488087 |
hgdp | rs488087 |
ensembl | rs488087 |
geneview | rs488087 |
scholar | rs488087 |
rs488087 | |
pharmgkb | rs488087 |
gwascentral | rs488087 |
openSNP | rs488087 |
23andMe | rs488087 |
SNPshot | rs488087 |
SNPdbe | rs488087 |
MSV3d | rs488087 |
GWAS Ctlg | rs488087 |
Max Magnitude | 0 |
[PMID 26498142] Rs488087 single nucleotide polymorphism as predictive risk factor for pancreatic cancers
ClinVar | |
---|---|
Risk | rs488087(T;T) |
Alt | rs488087(T;T) |
Reference | Rs488087(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CEL |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000009.11:g.135946599C>T |
CLNSRC | |
CLNACC | RCV000116657.2, |