SNP Report

Basic Info

Name	rs2681437 dbSNP Ensembl
Location	chr3:152321533 - 152321533(1)
Variant Alleles	A/G
Ancestral Allele	A
Minor Allele	G
Minor Allele Frequence	0.0493211
Functional Annotation	intron_variant.
Consequence to Transcript	intron_variant(ENST00000282486, ENST00000282488, ENST00000324196, ENST00000324210, ENST00000355460, ENST00000357472, ENST00000459747, ENST00000460591, ENST00000463374, ENST00000464596, ENST00000465907, ENST00000485509, ENST00000485910, ENST00000492948, ENST00000493459, ENST00000495875, ENST00000498502, ENST00000545754)
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 = 0.07596, Genotypic P-value = 0.00...... In GWAS: Allelic P-value = 0.07596, Genotypic P-value = 0.00752, Recessive P-value = 0.02326, HWE P-value = 0.24735; in Follow-up study: MAF=0.12, Allelic P-value = 0.01926, Allelic Q-value=0.5154, HWE P-value = 0.06182 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)
MBNL1	muscleblind-like splicing regulator 1	3q25	1(1/0/0)

SNPs in LD with rs2681437 (count: 0) View in gBrowse (chr3:152321533..152321533 )

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

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