rs10759944
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10759944(A;A) |
Make rs10759944(A;G) |
Make rs10759944(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 97794690 |
is a | snp |
is | mentioned by |
dbSNP | rs10759944 |
dbSNP (classic) | rs10759944 |
ClinGen | rs10759944 |
ebi | rs10759944 |
HLI | rs10759944 |
Exac | rs10759944 |
Gnomad | rs10759944 |
Varsome | rs10759944 |
LitVar | rs10759944 |
Map | rs10759944 |
PheGenI | rs10759944 |
Biobank | rs10759944 |
1000 genomes | rs10759944 |
hgdp | rs10759944 |
ensembl | rs10759944 |
geneview | rs10759944 |
scholar | rs10759944 |
rs10759944 | |
pharmgkb | rs10759944 |
gwascentral | rs10759944 |
openSNP | rs10759944 |
23andMe | rs10759944 |
SNPshot | rs10759944 |
SNPdbe | rs10759944 |
MSV3d | rs10759944 |
GWAS Ctlg | rs10759944 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25918370] Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer