SNP Report

Basic Info

Name	rs33976516 dbSNP Ensembl
Location	chr1:206110180 - 206110180(1)
Variant Alleles	G/C/T
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.0547125
Functional Annotation	3_prime_UTR_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	3_prime_UTR_variant(ENST00000367126); non_coding_transcript_exon_variant(ENST00000612906); non_coding_transcript_variant(ENST00000612906)
No. of Studies	1 (Positive: 1; Negative: 0; 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
Koefoed, P.,2011			Chi-square test: P-value = 0.013 Chi-square test: P-value = 0.013	Significant association was found in genotype association. Significant association was found in genotype association.	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
AVPR1B	arginine vasopressin receptor 1B	1q32	4(3/1/0)

SNPs in LD with rs33976516 (count: 0) View in gBrowse (chr1:206110180..206110180 )

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

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