SNP Report

Basic Info

Name	rs35449326 dbSNP Ensembl
Location	chr21:44525865 - 44525865(1)
Variant Alleles	G/A/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	7.98722E-4
Functional Annotation	intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000323084, ENST00000397916, ENST00000613245, ENST00000614657); non_coding_transcript_exon_variant(ENST00000465978); non_coding_transcript_variant(ENST00000465978)
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
McQuillin, A., 2006			no P-value no P-value	novel Polymorphisms identified in this study novel Polymorphisms identified in this study	Trend

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
C21orf90	TSPEAR antisense RNA 2	21q22.3	Mapped by Literature SNP
TSPEAR	thrombospondin-type laminin G domain and EAR repeats	21q22.3	Mapped by Literature SNP

SNPs in LD with rs35449326 (count: 0) View in gBrowse (chr21:44525865..44525865 )

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

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