SNP Report

Basic Info

Name	rs7119726 dbSNP Ensembl
Location	chr11:70612743 - 70612743(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.309105
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000338508, ENST00000357171, ENST00000409161, ENST00000409530, ENST00000412252, ENST00000426687, ENST00000445654, ENST00000449116, ENST00000449833, ENST00000601538); non_coding_transcript_variant(ENST00000445654)
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 = 0.000944, OR=1.57; for Iceland (replication sample): P-value = 0.045061, OR=0.86, Stouffer's z value=0.0025 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)
SHANK2	SH3 and multiple ankyrin repeat domains 2	11q13.2	2(1/1/0)

SNPs in LD with rs7119726 (count: 0) View in gBrowse (chr11:70612743..70612743 )

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

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