SNP Report

Basic Info

Name	rs181659924 dbSNP Ensembl
Location	chr2:75160594 - 75160594(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	1.99681E-4
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000305249, ENST00000409848, ENST00000604271); non_coding_transcript_variant(ENST00000604271)
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
Sharp S.I., 2014	C/T		P-value=0.03, OR=0.67, 95%CI=0.48-0.94 P-value=0.03, OR=0.67, 95%CI=0.48-0.94	Significant association was observed. Significant association was observed.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
TACR1	tachykinin receptor 1	2p13.1-p12	3(3/0/0)

SNPs in LD with rs181659924 (count: 0) View in gBrowse (chr2:75160594..75160594 )

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

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