SNP Report
Basic Info
Name |
rs10943465
dbSNP
Ensembl
|
Location |
Chr6:78236296(Fwd) |
Variant Alleles |
T/C |
Ancestral Allele |
T |
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] |
rs6298
|
synonymous_variant |
4(0/4/0)
|
0.913[CEU]; 0.843[CHD]; 0.834[GIH]; 0.866[JPT]; 0.89[MEX]; 0.884[TSI]
|
rs6296
|
synonymous_variant |
10(3/7/0)
|
0.912[CEU]; 0.842[CHD]; 0.877[GIH]; 0.86[JPT]; 0.946[MEX]; 0.884[TSI]
|
LD-proxies (count: 0)