SNP Report

Basic Info

Name	rs7610043 dbSNP Ensembl
Location	chr3:29346140 - 29346140(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.476438
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000273139, ENST00000383766, ENST00000383767, ENST00000434693, ENST00000445033, ENST00000452462, ENST00000456853, ENST00000471426, ENST00000635992, ENST00000636680, ENST00000637842); NMD_transcript_variant(ENST00000635992, ENST00000637842); non_coding_transcript_variant(ENST00000471426)
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
Baum, A. E., 2008 (a)		G	P-value = 0.0008 when genotyped individually in the test sam...... P-value = 0.0008 when genotyped individually in the test sample (NIMH); P-value = 0.124 when individually genotyped in the Replication sample (German); P-value = 0.001 in the combined dataset. OR (95% CI)=1.21 (1.08-1.35) More...		Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RBMS3	RNA binding motif, single stranded interacting protein 3	3p24-p23	1(0/1/0)

SNPs in LD with rs7610043 (count: 0) View in gBrowse (chr3:29346140..29346140 )

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

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