SNP Report

Basic Info

Name	rs10062367 dbSNP Ensembl
Location	chr5:76968529 - 76968529(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	A
Minor Allele Frequence	0.253794
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000274368, ENST00000503763, ENST00000514258); non_coding_transcript_variant(ENST00000503763, ENST00000514258)
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
Ceulemans, S.,2011	A/G		Single SNP analyses: Permuted P-value = 0.6691, Odds Ratio=1...... Single SNP analyses: Permuted P-value = 0.6691, Odds Ratio=1.063 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)
CRHBP	corticotropin releasing hormone binding protein	5q13.3	1(0/1/0)

SNPs in LD with rs10062367 (count: 0) View in gBrowse (chr5:76968529..76968529 )

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

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