SNP Report

Basic Info

Name	rs1705991 dbSNP Ensembl
Location	chr3:194653104 - 194653104(1)
Variant Alleles	G/A/C
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.365815
Functional Annotation	synonymous_variant; upstream_gene_variant.
Consequence to Transcript	synonymous_variant(ENST00000265245); upstream_gene_variant(ENST00000437613, ENST00000460584, ENST00000461343, ENST00000466391)
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
Schosser, A.,2011			chi-square (X²) test: genotype, X²=0.1...... chi-square (X²) test: genotype, X²=0.133, P-value = 0.936; allele, X²=0, P-value = 0.984 More...	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)
LSG1	large 60S subunit nuclear export GTPase 1	3q29	1(0/1/0)

SNPs in LD with rs1705991 (count: 0) View in gBrowse (chr3:194653104..194653104 )

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

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