SNP Report

Basic Info

Name	rs1073382 dbSNP Ensembl
Location	chr14:57736433 - 57736433(1)
Variant Alleles	T/G
Ancestral Allele	T
Minor Allele	T
Minor Allele Frequence	0.365016
Functional Annotation	intron_variant; non_coding_transcript_variant.
Consequence to Transcript	intron_variant(ENST00000556568, ENST00000556826, ENST00000557430); non_coding_transcript_variant(ENST00000556568, ENST00000557430)
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
Hattori, E.,2009			In GWAS: Allelic P-value = 0.06546, Genotypic P-value = 0.02...... In GWAS: Allelic P-value = 0.06546, Genotypic P-value = 0.02049, Recessive P-value = 0.0085, HWE P-value = 0.39121; in Follow-up study: MAF=0.42, Allelic P-value = 0.01909, Allelic Q-value=0.5154, HWE P-value = 0.24094 More...	Significant association was observed in both GWAS and Follow...... Significant association was observed in both GWAS and Follow-up study. More...	Positive

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
SLC35F4	solute carrier family 35, member F4	14q22.3	Mapped by Literature SNP

SNPs in LD with rs1073382 (count: 0) View in gBrowse (chr14:57736433..57736433 )

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

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