SNP Report
Basic Info
Name |
rs10120476
dbSNP
Ensembl
|
Location |
Chr9:110999316(Fwd) |
Variant Alleles |
C/T |
Ancestral Allele |
C |
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: 3)
rs_ID |
Functional Annotation |
r2[population] |
rs10979318
|
|
1.0[CHB]
|
rs12344381
|
|
1.0[CHD]
|
rs7860622
|
|
0.816[ASW]; 1.0[CHD]; 1.0[GIH]; 0.935[LWK]; 0.925[MKK]; 0.841[YRI]
|