SNP Report

Basic Info

Name	rs8021692 dbSNP Ensembl
Location	chr14:103962239 - 103962239(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.266174
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000409874, ENST00000496087, ENST00000554571); non_coding_transcript_variant(ENST00000496087, ENST00000554571)
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)=0.00000298, P-...... Non-weighted test under H0: P-value(additive)=0.00000298, P-value(dominant)=0.00000362, P-value(recessive)=0.0167; weighted test under H'0: P-value(additive)=0.000016, P-value(dominant)=0.0000197, P-value(recessive)=0.00939; logistic regression: P-value(additive)=0.00000364, P-value(dominant)=0.00000948, P-value(recessive)=0.00758 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)
TDRD9	tudor domain containing 9	14q32.33	3(1/1/1)

SNPs in LD with rs8021692 (count: 0) View in gBrowse (chr14:103962239..103962239 )

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

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