SNP Report
Basic Info
Name |
rs7860740
dbSNP
Ensembl
|
Location |
Chr9:93427347(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
G |
No. of Studies |
0 (significant: 0; non-significant: 0; trend: 0) |
Source |
LD-proxy
|
SNP related studies (count: 0)
SNP related genes (count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
Literature-origin SNPs (count: 2)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1412005
|
upstream_gene_variant |
1(1/0/0)
|
0.882[ASW]; 1.0[CEU]; 1.0[CHB]; 0.9[CHD]; 0.947[GIH]; 0.952[JPT]; 0.956[LWK]; 0.956[MEX]; 1.0[TSI]; 0.929[YRI]
|
rs1331503
|
intron_variant |
1(1/0/0)
|
0.955[CHB]; 0.907[JPT]
|
LD-proxies (count: 0)