SNP Report

Basic Info
| Name |
rs7383287
dbSNP
Ensembl
|
| Location |
chrCHR_HSCHR6_MHC_SSTO_CTG1:32906186 - 32906186(1) |
| Variant Alleles |
A/G |
| Ancestral Allele |
A |
| Minor Allele |
G |
| Minor Allele Frequence |
0.132388 |
| Functional Annotation |
intron_variant; NMD_transcript_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant; synonymous_variant.
|
| Consequence to Transcript |
intron_variant(ENST00000452392, ENST00000488325); NMD_transcript_variant(ENST00000488325); non_coding_transcript_exon_variant(ENST00000475235); non_coding_transcript_variant(ENST00000475235); synonymous_variant(ENST00000438763, ENST00000447394, ENST00000463161, ENST00000463161, ENST00000483576, ENST00000483576, ENST00000426644, ENST00000453971, ENST00000465683, ENST00000465683, ENST00000474748, ENST00000474748, ENST00000439310, ENST00000447178, ENST00000474604, ENST00000474604, ENST00000469995, ENST00000469995, ENST00000413252, ENST00000454286, ENST00000477041, ENST00000477041, ENST00000475173, ENST00000475173, ENST00000448690, ENST00000454969, ENST00000472450, ENST00000486158, ENST00000486158, ENST00000455155, ENST00000456406, ENST00000527042) |
| No. of Studies |
1 (Positive: 1; Negative: 0; Trend: 0) |
| Source |
Literature |
| Overlap with SZ? |
YES
|
| Overlap with MDD? |
NO
|

SNP related studies (count: 1)

SNP related genes (count: 1)

Overlap with SZ from cross-disorder studies (count: 1)
| Reference |
Statistical Result |
Description |
Result Category |
| Andreassen OA, 2013 |
Conditional FDR; SCZ loci given BD: P-value=0.0000271, FDR=0.095, FDR=0.019 for SCZ and BD |
To estimate the number of independent loci, we 'pruned' the associated SNPs (removed SNPs with linkage disequilibrium (LD)>0.2), and identified a total of 58 independent loci with a significance threshold of conditional FDR<0.32. |
Positive |

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