SNP Report

Basic Info

Name	rs697112 dbSNP Ensembl
Location	chr5:53964849 - 53964849(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.459265
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000502271, ENST00000504924, ENST00000507646, ENST00000510591, ENST00000620747); non_coding_transcript_variant(ENST00000510591)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
Forstner, A. J., 2015			P-value=3.61E-6 P-value=3.61E-6	After correction for multiple testing, nine miRNAs showed a ...... After correction for multiple testing, nine miRNAs showed a significant association with BD. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ARL15	ADP-ribosylation factor-like 15	5p15.2	Mapped by Literature SNP

SNPs in LD with rs697112 (count: 0) View in gBrowse (chr5:53964849..53964849 )

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

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