SNP Report

Basic Info

Name	rs8192627 dbSNP Ensembl
Location	chr6:132553675 - 132553675(1)
Variant Alleles	A/C/T
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.0421326
Functional Annotation	missense_variant. Polyphen Annotation: benign(ENST00000275200) SIFT Annotation: tolerated(ENST00000275200' target='_blank'>ENST00000275200); deleterious(ENST00000275200' target='_blank'>ENST00000275200)
Consequence to Transcript	missense_variant(ENST00000275200, ENST00000275200)
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
Abou Jamra, R.,2005(b)	A/C		In family base study: TDT P-value = 0.760 In family base study: TDT P-value = 0.760	No significant association was observed. No significant association was observed.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
TAAR8	trace amine associated receptor 8	6q23.2	1(0/1/0)

SNPs in LD with rs8192627 (count: 0) View in gBrowse (chr6:132553675..132553675 )

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

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