SNP Report

Basic Info

Name	rs517811 dbSNP Ensembl
Location	chr8:101932635 - 101932635(1)
Variant Alleles	G/A
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.40635
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000311028, ENST00000395923, ENST00000517531, ENST00000517639, ENST00000517822, ENST00000518166, ENST00000518661, ENST00000518727, ENST00000518952, ENST00000520425, ENST00000520690, ENST00000521599, ENST00000521964, ENST00000522078, ENST00000522206, ENST00000523923, ENST00000524209); non_coding_transcript_variant(ENST00000517639, ENST00000518952)
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
Xu, W., 2014			P(unadj)-value=0.001183,Â OR (unadj)=0.8009,Â P(adj)-value=0...... P(unadj)-value=0.001183,Â OR (unadj)=0.8009,Â P(adj)-value=0.001368,Â OR(adj)=0.7982 More...	Listing suggestive significant genic SNPs for combined Toron...... Listing suggestive significant genic SNPs for combined Toronto and London GWAS for which there are 4 or more suggestive significant SNPs among the top 1000, and for which no other positive reports have been published to date. More...	Negative

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
NCALD	neurocalcin delta	8q22.3	1(0/1/0)

SNPs in LD with rs517811 (count: 0) View in gBrowse (chr8:101932635..101932635 )

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

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