SNP Report
Basic Info
Name |
rs11118120
dbSNP
Ensembl
|
Location |
Chr1:218705761(Fwd) |
Variant Alleles |
A/C |
Ancestral Allele |
C |
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: 1)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1018040
|
|
1(0/0/1)
|
0.923[CEU]; 1.0[CHB]; 0.896[CHD]; 0.97[GIH]; 1.0[JPT]; 1.0[MEX]; 1.0[TSI]
|
LD-proxies (count: 0)