SNP Report

Basic Info

Name	rs12278912 dbSNP Ensembl
Location	chr11:124742263 - 124742263(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.307508
Functional Annotation	downstream_gene_variant; intron_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000531241); intron_variant(ENST00000284292, ENST00000412681)
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
Wen, Z., 2016	A/G		P-value=0.0512,Â OR=0.865, 95%CI=0.748â€“1.001 P-value=0.0512,Â OR=0.865, 95%CI=0.748â€“1.001	For bipolar disorder, rs7113041 and rs12278912 showed alleli...... For bipolar disorder, rs7113041 and rs12278912 showed allelic or genotypic association before Bonferroni correction. After Bonferroni correction, only rs7113041 remained associated with bipolar disorder. More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NRGN	neurogranin (protein kinase C substrate, RC3)	11q24	2(1/1/0)

SNPs in LD with rs12278912 (count: 0) View in gBrowse (chr11:124742263..124742263 )

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

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