SNP Report

Basic Info

Name	rs7247513 dbSNP Ensembl
Location	chr19:12580371 - 12580371(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.428514
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000311437, ENST00000593682); downstream_gene_variant(ENST00000414906, ENST00000440366, ENST00000465656); NMD_transcript_variant(ENST00000593682)
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)=0.00000207, P-...... Non-weighted test under H0: P-value(additive)=0.00000207, P-value(dominant)=0.0000894, P-value(recessive)=0.000108; weighted test under H'0: P-value(additive)=0.00000554, P-value(dominant)=0.000202, P-value(recessive)=0.00011; logistic regression: P-value(additive)=0.00000396, P-value(dominant)=0.00019, P-value(recessive)=0.0000919 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)
ZNF490	zinc finger protein 490	19p13.2	1(1/0/0)

SNPs in LD with rs7247513 (count: 0) View in gBrowse (chr19:12580371..12580371 )

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

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