rs10771279
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10771279(C;C) |
Make rs10771279(C;T) |
Make rs10771279(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 26377610 |
Gene | ITPR2 |
is a | snp |
is | mentioned by |
dbSNP | rs10771279 |
dbSNP (classic) | rs10771279 |
ClinGen | rs10771279 |
ebi | rs10771279 |
HLI | rs10771279 |
Exac | rs10771279 |
Gnomad | rs10771279 |
Varsome | rs10771279 |
LitVar | rs10771279 |
Map | rs10771279 |
PheGenI | rs10771279 |
Biobank | rs10771279 |
1000 genomes | rs10771279 |
hgdp | rs10771279 |
ensembl | rs10771279 |
geneview | rs10771279 |
scholar | rs10771279 |
rs10771279 | |
pharmgkb | rs10771279 |
gwascentral | rs10771279 |
openSNP | rs10771279 |
23andMe | rs10771279 |
SNPshot | rs10771279 |
SNPdbe | rs10771279 |
MSV3d | rs10771279 |
GWAS Ctlg | rs10771279 |
GMAF | 0.4945 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24220910] A genome-wide association study of renal cell carcinoma among African Americans