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: 16)
rs_ID |
Functional Annotation |
r2[population] |
rs8182163
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.911[CHD]; 1.0[JPT]
|
rs11150553
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 1.0[JPT]
|
rs7185268
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 1.0[JPT]
|
rs11647463
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.911[CHD]
|
rs750145
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHD]; 1.0[JPT]
|
rs889730
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
0.911[CHD]; 1.0[JPT]
|
rs11150550
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.814[CHD]
|
rs11646932
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 1.0[JPT]
|
rs11646944
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 1.0[JPT]
|
rs4564551
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[JPT]
|
rs12716966
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]
|
rs10514587
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.911[CHD]; 1.0[JPT]
|
rs11640229
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
0.823[CHB]; 1.0[JPT]
|
rs12325628
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.814[CHD]
|
rs7185229
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]; 0.911[CHD]; 1.0[JPT]
|
rs11864551
|
NMD_transcript_variant; intron_variant; nc_transcript_variant |
1.0[CHB]
|