rs6970262
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6970262(A;A) |
Make rs6970262(A;G) |
Make rs6970262(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 55192070 |
Gene | EGFR |
is a | snp |
is | mentioned by |
dbSNP | rs6970262 |
dbSNP (classic) | rs6970262 |
ClinGen | rs6970262 |
ebi | rs6970262 |
HLI | rs6970262 |
Exac | rs6970262 |
Gnomad | rs6970262 |
Varsome | rs6970262 |
LitVar | rs6970262 |
Map | rs6970262 |
PheGenI | rs6970262 |
Biobank | rs6970262 |
1000 genomes | rs6970262 |
hgdp | rs6970262 |
ensembl | rs6970262 |
geneview | rs6970262 |
scholar | rs6970262 |
rs6970262 | |
pharmgkb | rs6970262 |
gwascentral | rs6970262 |
openSNP | rs6970262 |
23andMe | rs6970262 |
SNPshot | rs6970262 |
SNPdbe | rs6970262 |
MSV3d | rs6970262 |
GWAS Ctlg | rs6970262 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25511740] Identification of epidermal growth factor receptor (EGFR) genetic variants that modify risk for head and neck squamous cell carcinoma
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 7
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d