SNP Report

Basic Info
Name |
rs10408146
dbSNP
Ensembl
|
Location |
Chr19:57735816(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: 1)
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] |
rs10421632
|
missense_variant |
1(0/0/1)
|
0.862[CHB]; 0.844[CHD]
|
rs2014572
|
5_prime_UTR_variant; missense_variant |
1(0/0/1)
|
0.863[CHB]
|
LD-proxies (count: 0)