rs17780102
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17780102(A;A) |
Make rs17780102(A;G) |
Make rs17780102(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 3599443 |
is a | snp |
is | mentioned by |
dbSNP | rs17780102 |
dbSNP (classic) | rs17780102 |
ClinGen | rs17780102 |
ebi | rs17780102 |
HLI | rs17780102 |
Exac | rs17780102 |
Gnomad | rs17780102 |
Varsome | rs17780102 |
LitVar | rs17780102 |
Map | rs17780102 |
PheGenI | rs17780102 |
Biobank | rs17780102 |
1000 genomes | rs17780102 |
hgdp | rs17780102 |
ensembl | rs17780102 |
geneview | rs17780102 |
scholar | rs17780102 |
rs17780102 | |
pharmgkb | rs17780102 |
gwascentral | rs17780102 |
openSNP | rs17780102 |
23andMe | rs17780102 |
SNPshot | rs17780102 |
SNPdbe | rs17780102 |
MSV3d | rs17780102 |
GWAS Ctlg | rs17780102 |
GMAF | 0.3779 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 22688887] Insight in glioma susceptibility through an analysis of 6p22.3, 12p13.33-12.1, 17q22-23.2 and 18q23 SNP genotypes in familial and non-familial glioma