SNP Report

Basic Info

Name	rs34796699 dbSNP Ensembl
Location	chr10:60196629 - 60196629(1)
Variant Alleles	A/-
Ancestral Allele	A
Minor Allele Frequence	0.0
Functional Annotation	intron_variant; NMD_transcript_variant; splice_region_variant.
Consequence to Transcript	intron_variant(ENST00000280772, ENST00000373827, ENST00000503366, ENST00000622427); NMD_transcript_variant(ENST00000622427); splice_region_variant(ENST00000280772, ENST00000373827, ENST00000503366, ENST00000622427)
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
Fiorentino A., 2014	-/A		eurMLP=11.33 eurMLP=11.33	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)
ANK3	ankyrin 3, node of Ranvier (ankyrin G)	10q21	17(13/3/1)

SNPs in LD with rs34796699 (count: 0) View in gBrowse (chr10:60196629..60196629 )

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

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