SNP Report

Basic Info
| Name |
rs2235698
dbSNP
Ensembl
|
| Location |
chrCHR_HSCHR6_MHC_QBL_CTG1:29587920 - 29587920(1) |
| Variant Alleles |
A/G |
| Ancestral Allele |
A |
| Minor Allele |
G |
| Minor Allele Frequence |
0.26897 |
| Functional Annotation |
downstream_gene_variant; intron_variant; synonymous_variant.
|
| Consequence to Transcript |
downstream_gene_variant(ENST00000441979); intron_variant(ENST00000355973); synonymous_variant(ENST00000383640, ENST00000441976, ENST00000449163, ENST00000453513, ENST00000441745, ENST00000438094, ENST00000439874, ENST00000424801, ENST00000417759, ENST00000411574, ENST00000439361, ENST00000448754, ENST00000454628, ENST00000417611, ENST00000383543, ENST00000383546, ENST00000453334, ENST00000383639, ENST00000376947) |
| No. of Studies |
1 (Positive: 0; Negative: 1; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| 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: 3)

| rs_ID |
Literature-origin SNPs with LD |
Functional Annotation |
r2[population] |
|
rs29221
|
|
downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]; 0.874[TSI]
|
|
rs29220
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CEU]
|
|
rs362522
|
|
downstream_gene_variant; intron_variant; upstream_gene_variant |
1.0[CEU]; 0.874[TSI]
|

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Bergen, S. E.,2012 |
logistic regression:for SZ full sample, OR=0.8, P-value = 8.59E-06 |
No significant association was observed in SZ. |
Negative |

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