SNP Report

Basic Info
Name |
rs2103119
dbSNP
Ensembl
|
Location |
Chr1:80197572(Fwd) |
Variant Alleles |
T/C |
Ancestral Allele |
C |
No. of Studies |
0 (significant: 0; non-significant: 0; trend: 0) |
Source |
LD-proxy
|

SNP related studies (count: 0)

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: 4)

|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1524174
|
|
1(0/1/0)
|
0.827[GIH]
|
rs7543390
|
|
1(0/1/0)
|
1.0[ASW]; 0.866[CEU]; 1.0[GIH]; 0.823[JPT]; 1.0[LWK]; 1.0[MKK]; 1.0[TSI]; 1.0[YRI]
|
rs6672282
|
|
1(0/0/1)
|
0.889[GIH]; 0.823[JPT]
|
rs6424669
|
|
1(0/1/0)
|
1.0[ASW]; 0.866[CEU]; 1.0[GIH]; 0.823[JPT]; 1.0[LWK]; 1.0[MKK]; 1.0[TSI]; 1.0[YRI]
|
LD-proxies (count: 0)