rs1729786
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1729786(A;A) |
Make rs1729786(A;G) |
Make rs1729786(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 95170985 |
Gene | ABCC4 |
is a | snp |
is | mentioned by |
dbSNP | rs1729786 |
dbSNP (classic) | rs1729786 |
ClinGen | rs1729786 |
ebi | rs1729786 |
HLI | rs1729786 |
Exac | rs1729786 |
Gnomad | rs1729786 |
Varsome | rs1729786 |
LitVar | rs1729786 |
Map | rs1729786 |
PheGenI | rs1729786 |
Biobank | rs1729786 |
1000 genomes | rs1729786 |
hgdp | rs1729786 |
ensembl | rs1729786 |
geneview | rs1729786 |
scholar | rs1729786 |
rs1729786 | |
pharmgkb | rs1729786 |
gwascentral | rs1729786 |
openSNP | rs1729786 |
23andMe | rs1729786 |
SNPshot | rs1729786 |
SNPdbe | rs1729786 |
MSV3d | rs1729786 |
GWAS Ctlg | rs1729786 |
GMAF | 0.2934 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 21792076] Systematic evaluation of genetic variants in three biological pathways on patient survival in low-stage non-small cell lung cancer