SNP Report

Basic Info
| Name |
rs11872481
dbSNP
Ensembl
|
| Location |
chr18:9128455 - 9128455(1) |
| Variant Alleles |
G/A |
| Ancestral Allele |
G |
| Minor Allele |
A |
| Minor Allele Frequence |
0.0754792 |
| Functional Annotation |
intron_variant; non_coding_transcript_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000318388, ENST00000400033, ENST00000465096, ENST00000474740, ENST00000578850, ENST00000579126, ENST00000582375, ENST00000583081); non_coding_transcript_variant(ENST00000465096, ENST00000474740, ENST00000578850, ENST00000579126, ENST00000582375, ENST00000583081) |
| No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
NO
|
| Overlap with MDD? |
NO
|

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: 19)

| rs_ID |
Literature-origin SNPs with LD |
Functional Annotation |
r2[population] |
|
rs12455304
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.89[CEU]
|
|
rs7229685
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.891[CEU]
|
|
rs12966775
|
|
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant |
1.0[CEU]
|
|
rs11660889
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.899[CEU]
|
|
rs11872176
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.9[CEU]
|
|
rs12454497
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.891[CEU]
|
|
rs12966444
|
|
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant |
0.89[CEU]
|
|
rs12968060
|
|
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant |
1.0[CEU]
|
|
rs11877843
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant |
0.9[CEU]
|
|
rs8085549
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|
|
rs10502390
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant |
1.0[CEU]
|
|
rs11081463
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|
|
rs11663949
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|
|
rs1046491
|
|
3_prime_UTR_variant |
0.89[CEU]
|
|
rs12454025
|
|
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant |
0.866[CEU]
|
|
rs11663175
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|
|
rs7226632
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant |
0.9[CEU]
|
|
rs11661921
|
|
downstream_gene_variant; intron_variant; non_coding_transcript_variant; upstream_gene_variant |
0.9[CEU]
|
|
rs11081459
|
|
downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)