SNP Report
Basic Info
Name |
rs2323262
dbSNP
Ensembl
|
Location |
Chr4:22144436(Fwd) |
Variant Alleles |
G/A |
Ancestral Allele |
G |
Functional Annotation |
intron_variant; nc_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000510705) nc_transcript_variant(ENST00000510705) |
No. of Studies |
2 (significant: 0; non-significant: 2; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 2)
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: 13)
rs_ID |
Functional Annotation |
r2[population] |
rs6826498
|
intron_variant; nc_transcript_variant |
1.0[ASW]; 0.973[GIH]; 1.0[JPT]; 1.0[LWK]; 1.0[MEX]; 0.888[MKK]; 0.899[TSI]
|
rs2323308
|
intron_variant; nc_transcript_variant |
0.876[MEX]
|
rs16872408
|
intron_variant; nc_transcript_variant |
0.919[GIH]; 0.821[MEX]
|
rs17528275
|
downstream_gene_variant; intron_variant; nc_transcript_variant |
0.946[GIH]; 0.937[MEX]
|
rs7669791
|
intron_variant; nc_transcript_variant |
0.919[GIH]; 0.821[MEX]
|
rs10019171
|
intron_variant; nc_transcript_variant |
0.919[GIH]; 0.821[MEX]
|
rs4334741
|
intron_variant; nc_transcript_variant |
1.0[JPT]
|
rs4410519
|
intron_variant; nc_transcript_variant |
0.973[GIH]; 1.0[JPT]; 1.0[MEX]; 0.899[TSI]
|
rs7664665
|
intron_variant; nc_transcript_variant |
0.919[GIH]; 0.821[MEX]
|
rs6818210
|
intron_variant; nc_transcript_variant |
0.946[GIH]; 0.821[MEX]
|
rs11728484
|
intron_variant; nc_transcript_variant |
0.802[CHB]; 0.824[JPT]
|
rs11933151
|
intron_variant; nc_transcript_variant |
0.883[MEX]
|
rs4697267
|
intron_variant; nc_transcript_variant |
0.946[GIH]; 0.821[MEX]
|