SNP Report

Basic Info

Name	rs3170633 dbSNP Ensembl
Location	chr1:93885772 - 93885772(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.420327
Functional Annotation	3_prime_UTR_variant; downstream_gene_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000370238); downstream_gene_variant(ENST00000615724)
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
Fullerton, J. M.,2010		T	Allelic association: X²=1.465, P-value = 0.226, O...... Allelic association: X²=1.465, P-value = 0.226, OR=0.871 for broad model; X²=1.704, P-value = 0.192, OR=0.848 More...	No significant association was observed in BD. No significant association was observed in BD.	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GCLM	glutamate-cysteine ligase, modifier subunit	1p21	1(0/0/1)

SNPs in LD with rs3170633 (count: 0) View in gBrowse (chr1:93885772..93885772 )

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

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