SNP Report

Basic Info
Name |
rs301410
dbSNP
Ensembl
|
Location |
chr19:8815355(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
G |
No. of Studies |
1 (significant: 0; non-significant: 1; trend: 0) |
Source |
Literature-origin
|

SNP related studies (count: 1)

SNP related genes (count: 0)
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: 10)

rs_ID |
Functional Annotation |
r2[population] |
rs301415
|
|
0.849[CEU]; 0.927[GIH]; 0.802[MKK]; 0.903[YRI]
|
rs10410943
|
missense_variant |
0.928[CHB]; 0.833[CHD]; 1.0[JPT]
|
rs2340550
|
missense_variant |
0.857[CHB]; 1.0[JPT]
|
rs2967682
|
upstream_gene_variant |
0.888[JPT]
|
rs2972524
|
|
0.888[JPT]
|
rs301412
|
|
0.928[CHB]; 0.833[CHD]; 1.0[JPT]
|
rs768896
|
|
0.888[JPT]
|
rs2967674
|
downstream_gene_variant |
0.888[JPT]
|
rs301420
|
|
0.889[CEU]; 1.0[CHB]; 1.0[JPT]
|
rs301409
|
|
0.928[CHB]; 0.833[CHD]; 1.0[JPT]
|