rs4975596
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4975596(A;A) |
Make rs4975596(A;G) |
Make rs4975596(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 1189232 |
is a | snp |
is | mentioned by |
dbSNP | rs4975596 |
dbSNP (classic) | rs4975596 |
ClinGen | rs4975596 |
ebi | rs4975596 |
HLI | rs4975596 |
Exac | rs4975596 |
Gnomad | rs4975596 |
Varsome | rs4975596 |
LitVar | rs4975596 |
Map | rs4975596 |
PheGenI | rs4975596 |
Biobank | rs4975596 |
1000 genomes | rs4975596 |
hgdp | rs4975596 |
ensembl | rs4975596 |
geneview | rs4975596 |
scholar | rs4975596 |
rs4975596 | |
pharmgkb | rs4975596 |
gwascentral | rs4975596 |
openSNP | rs4975596 |
23andMe | rs4975596 |
SNPshot | rs4975596 |
SNPdbe | rs4975596 |
MSV3d | rs4975596 |
GWAS Ctlg | rs4975596 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24152305] Association of candidate single nucleotide polymorphisms with somatic mutation of the epidermal growth factor receptor pathway