SNP Report

Basic Info

Name	rs17483687 dbSNP Ensembl
Location	chr4:148160841 - 148160841(1)
Variant Alleles	A/C
Ancestral Allele	A
Minor Allele	C
Minor Allele Frequence	0.0219649
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000342437, ENST00000344721, ENST00000358102, ENST00000503313, ENST00000511528, ENST00000512865, ENST00000514843, ENST00000625323); NMD_transcript_variant(ENST00000342437); non_coding_transcript_variant(ENST00000503313, ENST00000514843)
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	C/A		Single SNP analyses: Permuted P-value = 0.761, Odds Ratio=1....... Single SNP analyses: Permuted P-value = 0.761, Odds Ratio=1.075 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)
NR3C2	nuclear receptor subfamily 3, group C, member 2	4q31	1(1/0/0)

SNPs in LD with rs17483687 (count: 0) View in gBrowse (chr4:148160841..148160841 )

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

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