SNP Report
Basic Info
Name |
rs7995215
dbSNP
Ensembl
|
Location |
Chr13:94408506(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
G |
Functional Annotation |
intron_variant.
|
Consequence to Transcript |
intron_variant(ENST00000377047) |
No. of Studies |
1 (significant: 0; non-significant: 0; trend: 1) |
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: 15)
rs_ID |
Functional Annotation |
r2[population] |
rs7326722
|
intron_variant |
1.0[ASW]; 0.88[CEU]; 1.0[CHB]; 0.963[CHD]; 0.947[GIH]; 1.0[JPT]; 0.844[TSI]
|
rs4366594
|
intron_variant |
1.0[ASW]; 0.96[CEU]; 1.0[CHB]; 1.0[CHD]; 0.974[GIH]; 1.0[JPT]; 1.0[MEX]; 0.955[TSI]
|
rs9524187
|
intron_variant |
0.801[CEU]; 0.856[JPT]; 0.912[MEX]; 0.824[TSI]
|
rs7337988
|
intron_variant |
0.819[CHB]
|
rs4558277
|
intron_variant |
1.0[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs4773761
|
intron_variant |
0.87[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs4337169
|
intron_variant |
1.0[ASW]; 1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 0.931[LWK]; 1.0[MEX]; 0.874[MKK]; 0.955[TSI]
|
rs3759424
|
intron_variant |
0.819[CHB]; 0.857[JPT]
|
rs4517643
|
intron_variant |
0.956[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs4597178
|
intron_variant |
0.844[CEU]
|
rs7992378
|
intron_variant |
0.819[CHB]; 0.857[JPT]
|
rs9301908
|
intron_variant |
0.819[CHB]
|
rs4389020
|
intron_variant |
1.0[ASW]; 1.0[CEU]; 1.0[CHB]; 0.973[GIH]; 1.0[JPT]; 0.899[LWK]; 0.869[MKK]
|
rs4275728
|
intron_variant |
0.909[CEU]
|
rs2389049
|
intron_variant |
0.819[CHB]; 0.857[JPT]
|