SNP Report

Basic Info

Name	rs2297354 dbSNP Ensembl
Location	chr9:90642058 - 90642058(1)
Variant Alleles	G/C
Ancestral Allele	G
Minor Allele	C
Minor Allele Frequence	0.0335463
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	C/G	G	X² test: P-value = 0.6345, OR=1.24, 95%CI=0.51-3....... X² test: P-value = 0.6345, OR=1.24, 95%CI=0.51-3.02 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 rs2297354 (count: 0) View in gBrowse (chr9:90642058..90642058 )

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

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