SNP Report

Basic Info

Name	rs690111 dbSNP Ensembl
Location	chr9:90615008 - 90615008(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.370208
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000375765, ENST00000636786, ENST00000637905)
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
Reif, A.,2011	G/T	T	X² test: P-value = 0.1752, OR=1.18, 95%CI=0.93-1....... X² test: P-value = 0.1752, OR=1.18, 95%CI=0.93-1.50 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)
DIRAS2	DIRAS family, GTP-binding RAS-like 2	9q22.32	1(1/0/0)

SNPs in LD with rs690111 (count: 1) View in gBrowse (chr9:90615008..90618490 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²<=0.8.

rs_ID	Literature-origin SNPs with LD	Functional Annotation	r²[population]
rs540870		intron_variant	0.826[TSI]

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

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