SNP Report

Basic Info

Name	rs2018783 dbSNP Ensembl
Location	chr10:60256024 - 60256024(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.45028
Functional Annotation	intron_variant; NMD_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000280772, ENST00000373827, ENST00000503366, ENST00000503925, ENST00000622427); NMD_transcript_variant(ENST00000622427)
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
Dedman, A.,2012	G/A		Association analysis: for UCL1 sample, P-value = 0.043, OR=1...... Association analysis: for UCL1 sample, P-value = 0.043, OR=1.2; for UCL2 sample, P-value = 0.92, OR=1.01; for UCL1+UCL2 sample, P-value = 0.089, OR=1.11 More...	Significant association was observed in BD. Significant association was observed in BD.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ANK3	ankyrin 3, node of Ranvier (ankyrin G)	10q21	17(13/3/1)

SNPs in LD with rs2018783 (count: 0) View in gBrowse (chr10:60256024..60256024 )

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

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