SNP Report
Basic Info
Name |
rs3027415
dbSNP
Ensembl
|
Location |
ChrX:43614441(Fwd) |
Variant Alleles |
T/C |
Ancestral Allele |
T |
No. of Studies |
1 (significant: 1; non-significant: 0; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 1)
SNP related genes (count: 1)
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: 0)
LD-proxies (count: 5)
rs_ID |
Functional Annotation |
r2[population] |
rs3027456
|
intron_variant; nc_transcript_variant |
0.894[MEX]
|
rs2283729
|
intron_variant; nc_transcript_variant |
0.894[MEX]
|
rs10521432
|
intron_variant |
0.893[MEX]
|
rs5905449
|
downstream_gene_variant; intron_variant |
1.0[ASW]; 0.922[CEU]; 1.0[CHB]; 0.827[GIH]; 1.0[MEX]; 0.955[TSI]
|
rs3027450
|
intron_variant |
1.0[ASW]; 0.922[CEU]; 1.0[CHB]; 0.827[GIH]; 1.0[MEX]; 0.955[TSI]
|