SNP Report
Basic Info
Name |
rs2311120
dbSNP
Ensembl
|
Location |
Chr18:52477123(Fwd) |
Variant Alleles |
A/G |
Ancestral Allele |
A |
Functional Annotation |
intron_variant.
|
Consequence to Transcript |
intron_variant(ENST00000586570) |
No. of Studies |
2 (significant: 0; non-significant: 2; trend: 0) |
Source |
Literature-origin
|
SNP related studies (count: 2)
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: 16)
rs_ID |
Functional Annotation |
r2[population] |
rs4800976
|
intron_variant; nc_transcript_variant |
0.816[CEU]; 0.898[CHB]
|
rs1978355
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]
|
rs2016584
|
intron_variant |
1.0[CEU]; 0.888[CHB]; 0.851[YRI]
|
rs9945547
|
intron_variant; upstream_gene_variant |
0.804[CEU]; 1.0[CHB]
|
rs1819888
|
intron_variant; nc_transcript_variant |
1.0[CEU]; 1.0[CHB]
|
rs9945718
|
intron_variant; upstream_gene_variant |
1.0[CHB]
|
rs1833284
|
intron_variant; nc_transcript_variant |
0.804[CEU]; 0.897[CHB]
|
rs12604321
|
intron_variant; nc_transcript_variant |
0.897[CHB]
|
rs2008739
|
intron_variant |
0.895[CEU]; 1.0[YRI]
|
rs4800977
|
intron_variant; nc_transcript_variant |
0.804[CEU]; 0.897[CHB]
|
rs2008315
|
intron_variant |
1.0[YRI]
|
rs1972593
|
intron_variant; nc_transcript_variant |
1.0[CHB]
|
rs1833283
|
intron_variant; nc_transcript_variant |
0.816[CEU]; 0.898[CHB]
|
rs2006776
|
intron_variant; nc_transcript_variant |
0.832[CEU]; 1.0[YRI]
|
rs2018485
|
intron_variant |
1.0[CHB]; 1.0[JPT]
|
rs1819887
|
intron_variant; nc_transcript_variant |
0.804[CEU]; 0.897[CHB]
|