SNP Report
Basic Info
Name |
rs972604
dbSNP
Ensembl
|
Location |
Chr9:87648729(Fwd) |
Variant Alleles |
C/T |
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: 2)
|
rs_ID |
Functional Annotation |
#studies(significant/non-significant/trend) |
r2[population] |
rs1387926
|
intron_variant |
1(1/0/0)
|
0.864[CHB]; 1.0[JPT]; 0.947[MEX]
|
rs1073049
|
|
1(1/0/0)
|
1.0[ASW]; 1.0[CEU]; 1.0[CHB]; 1.0[CHD]; 1.0[GIH]; 1.0[JPT]; 0.973[LWK]; 1.0[MEX]; 0.979[MKK]; 0.941[TSI]; 1.0[YRI]
|
LD-proxies (count: 0)