BDgene

SNP Report

Basic Info
Name rs7183870 dbSNP Ensembl
Location chr15:92057169 - 92057169(1)
Variant Alleles A/G
Ancestral Allele G
Minor Allele A
Minor Allele Frequence 0.390974
Functional Annotation intron_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000318445, ENST00000424469, ENST00000553653, ENST00000555769, ENST00000556649); non_coding_transcript_variant(ENST00000553653, ENST00000555769, ENST00000556649)
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 = 0.00151, OR=0.64 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)
SLCO3A1 solute carrier organic anion transporter family, member 3A1 15q26 2(1/1/0)

SNPs in LD with rs7183870 (count: 9) View in gBrowse (chr15:92055844..92070744 )
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: 9)


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

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