SNP Report

Basic Info
Name rs914715 dbSNP Ensembl
Location chr9:79695983 - 79695983(1)
Variant Alleles T/A
Ancestral Allele A
Minor Allele T
Minor Allele Frequence 0.0199681
Functional Annotation intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript intron_variant(ENST00000265284, ENST00000376537, ENST00000376544, ENST00000376552, ENST00000428713, ENST00000435650, ENST00000462803, ENST00000463431, ENST00000470872, ENST00000490347); NMD_transcript_variant(ENST00000462803, ENST00000470872); non_coding_transcript_variant(ENST00000463431)
No. of Studies 1 (Positive: 0; Negative: 0; Trend: 1)
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
Jiang, Y.,2011 Non-weighted test under H0: P-value(additive)=0.00000228, P-...... Non-weighted test under H0: P-value(additive)=0.00000228, P-value(dominant)=0.00000126, P-value(recessive)=0.956; weighted test under H'0: P-value(additive)=0.00000171, P-value(dominant)=0.00000214, P-value(recessive)=0.766; logistic regression: P-value(additive)=0.00000102, P-value(dominant)=0.000000705, P-value(recessive)=0.729 More... Suggestive association was found. Suggestive association was found. Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
TLE4 transducin-like enhancer of split 4 9q21.32 2(1/1/0)

SNPs in LD with rs914715 (count: 0) View in gBrowse (chr9:79695983..79695983 )

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

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