SNP Report

Basic Info
Name |
rs11142062
dbSNP
Ensembl
|
Location |
Chr9:90658749(Fwd) |
Variant Alleles |
C/T |
Ancestral Allele |
C |
No. of Studies |
1 (significant: 0; non-significant: 1; trend: 0) |
Source |
Literature-origin
|

SNP related studies (count: 1)

SNP related genes (count: 1)
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: 0)
LD-proxies (count: 1)

rs_ID |
Functional Annotation |
r2[population] |
rs11142056
|
|
1.0[CEU]
|