SNP Report

Basic Info
Name |
rs1427339
dbSNP
Ensembl
|
Location |
Chr2:108588292(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
A |
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: 1)

|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1013940
|
5_prime_UTR_variant; missense_variant |
1(1/0/0)
|
1.0[ASW]; 0.84[CHB]; 0.956[CHD]; 1.0[GIH]; 0.845[JPT]; 0.804[MEX]; 1.0[MKK]; 1.0[TSI]; 1.0[YRI]
|
LD-proxies (count: 0)