rs8048207
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8048207(C;C) |
Make rs8048207(C;T) |
Make rs8048207(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 61744191 |
Gene | CDH8 |
is a | snp |
is | mentioned by |
dbSNP | rs8048207 |
dbSNP (classic) | rs8048207 |
ClinGen | rs8048207 |
ebi | rs8048207 |
HLI | rs8048207 |
Exac | rs8048207 |
Gnomad | rs8048207 |
Varsome | rs8048207 |
LitVar | rs8048207 |
Map | rs8048207 |
PheGenI | rs8048207 |
Biobank | rs8048207 |
1000 genomes | rs8048207 |
hgdp | rs8048207 |
ensembl | rs8048207 |
geneview | rs8048207 |
scholar | rs8048207 |
rs8048207 | |
pharmgkb | rs8048207 |
gwascentral | rs8048207 |
openSNP | rs8048207 |
23andMe | rs8048207 |
SNPshot | rs8048207 |
SNPdbe | rs8048207 |
MSV3d | rs8048207 |
GWAS Ctlg | rs8048207 |
GMAF | 0.1506 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23144319] |
Trait | Non-small cell lung cancer |
Title | Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. |
Risk Allele | T |
P-val | 8E-6 |
Odds Ratio | NR NR |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 16
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d