SNP Report

Basic Info

Name	rs3735835 dbSNP Ensembl
Location	chr8:20164494 - 20164494(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.3125
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000265808, ENST00000276373, ENST00000381608, ENST00000437980, ENST00000440926, ENST00000517776, ENST00000519026); NMD_transcript_variant(ENST00000517776)
No. of Studies	1 (Positive: 1; Negative: 0; 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
Lohoff, F. W., 2006	G/C		genotypic P-value = 0.069, allelic P-value = 0.038 for BPI ;...... genotypic P-value = 0.069, allelic P-value = 0.038 for BPI ; genotypic P-value = 0.1, allelic P-value = 0.035 for BP I psychosis More...	This SNP is associated with the disease. This SNP is associated with the disease.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SLC18A1	solute carrier family 18 (vesicular monoamine transporter), member 1	8p21.3	3(2/1/0)

SNPs in LD with rs3735835 (count: 0) View in gBrowse (chr8:20164494..20164494 )

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

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