SNP Report

Basic Info

Name	rs17432461 dbSNP Ensembl
Location	chr15:36882755 - 36882755(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.0816693
Functional Annotation	intron_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000558089, ENST00000561259); non_coding_transcript_variant(ENST00000558089, ENST00000561259); upstream_gene_variant(ENST00000560602)
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
Xu, W., 2014	T/C		P-value=3.94E-05 P-value=3.94E-05	Top 132 SNPs (showing suggestive association to BD in our CA...... Top 132 SNPs (showing suggestive association to BD in our CAMH family cohort: p<0.0001). More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
LOC145845	uncharacterized LOC145845	15q14	1(0/1/0)

SNPs in LD with rs17432461 (count: 0) View in gBrowse (chr15:36882755..36882755 )

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

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