SNP Report

Basic Info

Name	rs1019385 dbSNP Ensembl
Location	chr12:13981909 - 13981909(1)
Variant Alleles	C/A
Ancestral Allele	C
Minor Allele	A
Minor Allele Frequence	0.428714
Functional Annotation	intron_variant; splice_region_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000627535, ENST00000630791); splice_region_variant(ENST00000627535, ENST00000630791); upstream_gene_variant(ENST00000609686, ENST00000637875)
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
Dalvie, S.,2010			SNP Allele Frequencies: logistic regression, for Caucasian, ...... SNP Allele Frequencies: logistic regression, for Caucasian, Mixed Ancestry, P-value = 0.8268; for Caucasian only, P-value = 0.9181; for Mixed Ancestry only, P-value = 0.8304 More...	No significant association was observed in BP-I. No significant association was observed in BP-I.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GRIN2B	glutamate receptor, ionotropic, N-methyl D-aspartate 2B	12p13.1	8(4/4/0)

SNPs in LD with rs1019385 (count: 0) View in gBrowse (chr12:13981909..13981909 )

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

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