SNP Report

Basic Info

Name	rs9401594 dbSNP Ensembl
Location	chr6:122782340 - 122782340(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.399561
Functional Annotation	3_prime_UTR_variant; intron_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000356535); intron_variant(ENST00000368444)
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
Iwayama, Y., 2010	T/C		P-value for allele test is 0.3594, p-value for genotype test...... P-value for allele test is 0.3594, p-value for genotype test is 0.6554, p-value is 0.9976 after correction by permutation test. More...		Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
FABP7	fatty acid binding protein 7, brain	6q22-q23	1(1/0/0)

SNPs in LD with rs9401594 (count: 1) View in gBrowse (chr6:122780502..122782340 )

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]
rs2243372		intron_variant	0.822[CHB]

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

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