SNP Report

Basic Info

Name	rs4764470 dbSNP Ensembl
Location	chr12:19189219 - 19189219(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.381789
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000299275, ENST00000429027, ENST00000535357, ENST00000538034, ENST00000538714, ENST00000539256, ENST00000540972); non_coding_transcript_variant(ENST00000535357, ENST00000538034)
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
Jamain, S., 2014		A	French sample:Â P-value=2.55E-04,Â OR=1.53;Â German sample:Â...... French sample:Â P-value=2.55E-04,Â OR=1.53;Â German sample:Â P-value=1.84E-02,Â OR=1.39;Â Meta-analysis:Â P-value_meta=1.73E-05,Â OR_meta=1.47 More...	This SNP showed a difference in allele frequencies at P<5E-0...... This SNP showed a difference in allele frequencies at P<5E-05. More...	Trend

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
AEBP2	AE binding protein 2	12p12.3	1(1/0/0)
PLEKHA5	pleckstrin homology domain containing, family A member 5	12p12	1(1/0/0)

SNPs in LD with rs4764470 (count: 0) View in gBrowse (chr12:19189219..19189219 )

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

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