SNP Report

Basic Info

Name	rs35106713 dbSNP Ensembl
Location	chr3:7146493 - 7146493(1)
Variant Alleles	T/C
Ancestral Allele	T
Minor Allele	C
Minor Allele Frequence	0.00479233
Functional Annotation	3_prime_UTR_variant; 5_prime_UTR_variant; NMD_transcript_variant; synonymous_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000435689, ENST00000443259); 5_prime_UTR_variant(ENST00000448328); NMD_transcript_variant(ENST00000389335, ENST00000435689, ENST00000440923, ENST00000443259, ENST00000467425); synonymous_variant(ENST00000357716, ENST00000389335, ENST00000389336, ENST00000440923, ENST00000467425, ENST00000486284)
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
Kandaswamy R., 2014	T/C		MAF=0.02; P-value=0.188; OR=0.64, 95%CI=0.33-1.25 MAF=0.02; P-value=0.188; OR=0.64, 95%CI=0.33-1.25	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)
GRM7	glutamate receptor, metabotropic 7	3p26-p25	3(2/1/0)

SNPs in LD with rs35106713 (count: 0) View in gBrowse (chr3:7146493..7146493 )

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

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