SNP Report

Basic Info
Name |
rs12679254
dbSNP
Ensembl
|
Location |
Chr8:74274191(Fwd) |
Variant Alleles |
C/T |
Ancestral Allele |
C |
Functional Annotation |
intron_variant; nc_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000518355; ENST00000519134) nc_transcript_variant(ENST00000518355; ENST00000519134) |
No. of Studies |
1 (significant: 0; non-significant: 0; trend: 1) |
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: 12)

rs_ID |
Functional Annotation |
r2[population] |
rs12334531
|
intron_variant; nc_transcript_variant |
0.839[MEX]
|
rs16938626
|
downstream_gene_variant |
0.896[CEU]; 0.951[CHB]; 0.953[JPT]
|
rs16938627
|
downstream_gene_variant |
0.901[CHB]; 0.846[GIH]; 0.909[JPT]; 0.834[MEX]
|
rs2383901
|
nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
0.908[CHB]; 0.815[JPT]
|
rs12548090
|
intron_variant; nc_transcript_variant; upstream_gene_variant |
0.908[CHB]
|
rs10957658
|
intron_variant; nc_transcript_variant; upstream_gene_variant |
0.862[CEU]; 0.862[CHB]; 1.0[YRI]
|
rs2383904
|
downstream_gene_variant |
0.953[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs12678600
|
intron_variant; nc_transcript_variant; upstream_gene_variant |
1.0[CEU]; 1.0[CHB]; 0.906[JPT]; 1.0[YRI]
|
rs2383903
|
downstream_gene_variant |
0.86[CEU]; 0.953[CHB]; 1.0[JPT]; 1.0[YRI]
|
rs1807080
|
upstream_gene_variant |
0.908[CHB]; 0.815[JPT]
|
rs13265054
|
upstream_gene_variant |
1.0[CEU]; 1.0[CHB]; 0.904[JPT]
|
rs16938624
|
intron_variant; nc_transcript_variant; upstream_gene_variant |
0.889[CEU]; 1.0[CHB]; 0.895[JPT]
|