SNP Report

Basic Info

Name	rs1408047 dbSNP Ensembl
Location	chr13:102832568 - 102832568(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	C
Minor Allele Frequence	0.429912
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000257336, ENST00000448849, ENST00000490317, ENST00000602836); non_coding_transcript_variant(ENST00000490317)
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
Ferraren, D. O.,2005		C	Assocaition study: TDT P-value = 1 for CNG Series, TDT P-val...... Assocaition study: TDT P-value = 1 for CNG Series, TDT P-value = 0.15 for NIMH 1 and 2; chi quare test P-value > 0.05 in case-control study More...	No significant association was observed in BD. No significant association was observed in BD.	Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
BIVM-ERCC5	BIVM-ERCC5 readthrough	13q33.1	Mapped by Literature SNP
BIVM	basic, immunoglobulin-like variable motif containing	13q33.1	Mapped by Literature SNP

SNPs in LD with rs1408047 (count: 0) View in gBrowse (chr13:102832568..102832568 )

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

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