SNP Report

Basic Info
Name |
rs1837232
dbSNP
Ensembl
|
Location |
chr3:165631805(Fwd) |
Variant Alleles |
G/A |
Ancestral Allele |
G |
No. of Studies |
1 (significant: 0; non-significant: 1; trend: 0) |
Source |
Literature-origin
|

SNP related studies (count: 1)

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: 0)
LD-proxies (count: 4)

rs_ID |
Functional Annotation |
r2[population] |
rs1355538
|
intron_variant; NMD_transcript_variant |
0.835[CHB]
|
rs282188
|
|
0.826[CHB]
|
rs282221
|
|
0.858[CHB]
|
rs4639017
|
intron_variant; NMD_transcript_variant |
0.835[CHB]; 0.83[JPT]
|