SNP Report
Basic Info
Name |
rs5951031
dbSNP
Ensembl
|
Location |
ChrX:43404656(Fwd) |
Variant Alleles |
C/T |
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: 4)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs5953210
|
upstream_gene_variant |
1(1/0/0)
|
0.876[CEU]; 0.884[TSI]
|
rs5905702
|
intron_variant; nc_transcript_variant |
1(0/1/0)
|
0.875[CEU]; 0.815[TSI]
|
rs4570308
|
upstream_gene_variant |
1(1/0/0)
|
0.876[CEU]
|
rs3788863
|
intron_variant; nc_transcript_variant |
1(1/0/0)
|
0.876[CEU]; 0.85[TSI]
|
LD-proxies (count: 0)