SNP Report

Basic Info

Name	rs8140359 dbSNP Ensembl
Location	chr22:25882727 - 25882727(1)
Variant Alleles	C/T
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.0385383
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000600211); intron_variant(ENST00000335473, ENST00000407587, ENST00000418374, ENST00000453457, ENST00000536101, ENST00000539302); NMD_transcript_variant(ENST00000539302); non_coding_transcript_variant(ENST00000418374, ENST00000453457)
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	A/G		P-value=7.44E-05 P-value=7.44E-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)
MYO18B	myosin XVIIIB	22q12.1	2(0/2/0)

SNPs in LD with rs8140359 (count: 0) View in gBrowse (chr22:25882727..25882727 )

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

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