SNP Report
Basic Info
Name |
rs1967630
dbSNP
Ensembl
|
Location |
ChrX:6959429(Fwd) |
Variant Alleles |
C/T |
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: 2)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1473666
|
downstream_gene_variant; intron_variant; nc_transcript_variant |
1(0/1/0)
|
1.0[CHD]; 1.0[GIH]
|
rs5934740
|
intron_variant |
2(0/2/0)
|
1.0[ASW]; 0.899[CEU]; 0.932[CHB]; 1.0[CHD]; 0.864[GIH]; 0.927[JPT]; 0.937[MEX]; 1.0[TSI]
|
LD-proxies (count: 0)