BDgene

SNP Report

Basic Info
Name rs931781 dbSNP Ensembl
Location chr15:48662707 - 48662707(1)
Variant Alleles A/T
Ancestral Allele T
Minor Allele A
Minor Allele Frequence 0.217652
Functional Annotation non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript non_coding_transcript_exon_variant(ENST00000616350); non_coding_transcript_variant(ENST00000616350)
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)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Djurovic, S.,2010 Combined analysis: for TOP Norway (discovery sample): P-valu...... Combined analysis: for TOP Norway (discovery sample): P-value = 0.000937, OR=0.61 More... No significant association was observed in BD. No significant association was observed in BD. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
FBN1 fibrillin 1 15q21.1 2(0/2/0)

SNPs in LD with rs931781 (count: 25) View in gBrowse (chr15:48656881..48697690 )
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: 25)


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

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