SNP Report
Basic Info
Name |
rs10799793
dbSNP
Ensembl
|
Location |
Chr1:23545787(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] |
rs676643
|
upstream_gene_variant |
1(1/0/0)
|
0.93[CEU]; 0.947[CHB]; 0.947[CHD]; 0.92[JPT]; 0.868[MKK]; 0.969[TSI]
|
rs604030
|
downstream_gene_variant; intron_variant |
1(1/0/0)
|
0.949[CHB]; 0.928[JPT]
|
LD-proxies (count: 0)