SNP Report

Basic Info

Name	rs16914794 dbSNP Ensembl
Location	chr10:60141024 - 60141024(1)
Variant Alleles	C/G
Ancestral Allele	C
Minor Allele	G
Minor Allele Frequence	0.102037
Functional Annotation	downstream_gene_variant; intron_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000633779); intron_variant(ENST00000280772, ENST00000373827, ENST00000460468, ENST00000474360, ENST00000503366, ENST00000622427); NMD_transcript_variant(ENST00000622427); upstream_gene_variant(ENST00000355288, ENST00000373815, ENST00000486349, ENST00000506635, ENST00000513049, ENST00000618080)
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	C/G		eurMLP=0.37 eurMLP=0.37	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 rs16914794 (count: 0) View in gBrowse (chr10:60141024..60141024 )

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

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