SNP Report
Basic Info
Name |
rs2910800
dbSNP
Ensembl
|
Location |
Chr5:37788642(Fwd) |
Variant Alleles |
T/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: 3)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1862574
|
intron_variant |
1(0/1/0)
|
0.849[CHB]; 0.89[JPT]
|
rs2216711
|
intron_variant |
1(0/1/0)
|
0.849[CHB]
|
rs3749692
|
3_prime_UTR_variant; downstream_gene_variant |
1(0/1/0)
|
0.874[CHD]
|
LD-proxies (count: 0)