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: 24)

rs_ID |
Functional Annotation |
r2[population] |
rs4730019
|
intron_variant |
1.0[CHB]; 0.944[JPT]
|
rs11972645
|
intron_variant |
0.899[CHB]; 0.857[JPT]
|
rs9987005
|
intron_variant |
0.91[CHB]; 0.866[JPT]
|
rs9656100
|
intron_variant |
0.863[CHB]; 0.809[CHD]; 0.953[JPT]
|
rs12535955
|
intron_variant |
0.954[CHB]; 0.866[JPT]
|
rs1989781
|
intron_variant |
0.908[CHB]; 0.821[CHD]; 0.953[JPT]
|
rs756667
|
intron_variant |
0.91[CHB]; 0.866[JPT]
|
rs7785646
|
intron_variant |
0.856[CHB]; 0.899[JPT]
|
rs2385173
|
intron_variant |
0.952[CHB]; 0.952[JPT]
|
rs6465995
|
intron_variant |
0.868[CHB]; 0.866[JPT]
|
rs6949801
|
intron_variant |
0.91[CHB]; 0.828[CHD]; 0.953[JPT]
|
rs7804269
|
intron_variant |
0.908[CHB]; 0.821[CHD]; 0.953[JPT]
|
rs2188170
|
intron_variant |
0.953[CHB]; 0.866[JPT]
|
rs2193203
|
intron_variant |
0.866[JPT]
|
rs756668
|
intron_variant |
0.954[CHB]; 0.846[CHD]; 0.953[JPT]
|
rs6465994
|
intron_variant |
0.841[TSI]; 0.954[CHB]; 0.954[CHD]; 1.0[JPT]; 0.972[GIH]; 0.852[LWK]; 0.855[MEX]; 0.887[MKK]; 1.0[YRI]
|
rs9656097
|
intron_variant |
0.952[CHB]; 0.949[JPT]
|
rs7783352
|
intron_variant |
0.91[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs10255529
|
intron_variant |
0.954[CHB]; 0.951[JPT]
|
rs12216618
|
intron_variant |
0.817[JPT]
|
rs7804412
|
intron_variant |
0.953[CHB]; 0.952[JPT]
|
rs9649272
|
intron_variant |
0.91[CHB]; 0.866[JPT]
|
rs17421541
|
intron_variant |
0.866[JPT]
|
rs1156368
|
intron_variant |
0.908[CHB]; 0.863[JPT]
|