SNP Report

Basic Info

Name	rs1893050 dbSNP Ensembl
Location	chr11:84917050 - 84917050(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.0165735
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000376104, ENST00000398309, ENST00000524982, ENST00000527088, ENST00000529111, ENST00000530589, ENST00000532653); non_coding_transcript_variant(ENST00000529111, ENST00000530589)
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
Xu, W., 2014	C/T		P-value=5.31E-05 P-value=5.31E-05	Top 132 SNPs (showing suggestive association to BD in our CA...... Top 132 SNPs (showing suggestive association to BD in our CAMH family cohort: p<0.0001). More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
DLG2	discs, large homolog 2 (Drosophila)	11q21	3(1/1/1)

SNPs in LD with rs1893050 (count: 0) View in gBrowse (chr11:84917050..84917050 )

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

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