SNP Report
Basic Info
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: 13)
rs_ID |
Functional Annotation |
r2[population] |
rs2848463
|
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]; 0.879[TSI]
|
rs2071139
|
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs2848455
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs2071138
|
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]; 0.879[TSI]
|
rs2586214
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs787559
|
intron_variant; nc_transcript_variant |
0.877[CHB]; 1.0[JPT]
|
rs2855646
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]; 0.856[CHD]; 0.919[GIH]; 1.0[JPT]; 0.905[MEX]; 1.0[TSI]
|
rs2859542
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 0.874[TSI]
|
rs2855639
|
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]
|
rs2586211
|
downstream_gene_variant; intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]; 0.856[CHD]; 1.0[GIH]; 1.0[JPT]; 1.0[TSI]
|
rs2848465
|
downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]; 1.0[CHB]; 0.856[CHD]; 0.896[GIH]; 1.0[JPT]; 0.905[MEX]; 1.0[TSI]
|
rs2071140
|
downstream_gene_variant; intron_variant; nc_transcript_variant |
1.0[CEU]
|
rs2848454
|
intron_variant; nc_transcript_variant |
1.0[JPT]
|