SNP Report

Basic Info

Name	rs137931 dbSNP Ensembl
Location	chr22:50085822 - 50085821(1)
Variant Alleles	-/C
Minor Allele	-
Minor Allele Frequence	0.328075
Functional Annotation	5_prime_UTR_variant; upstream_gene_variant.
Consequence to Transcript	5_prime_UTR_variant(ENST00000311597); upstream_gene_variant(ENST00000262794, ENST00000395854, ENST00000395858, ENST00000395876, ENST00000419054, ENST00000442311, ENST00000475190, ENST00000540615, ENST00000545383)
No. of Studies	1 (Positive: 0; Negative: 1; Trend: 0)
Source	Literature
Overlap with SZ?	YES
Overlap with MDD?	NO

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result Category
Severinsen, J. E., 2006 (b)	C/-		P-value = 0.2842 in BD, P-value = 0.5796 in BD and SZ P-value = 0.2842 in BD, P-value = 0.5796 in BD and SZ		Negative

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
MOV10L1	Mov10 RISC complex RNA helicase like 1	22q13.33	1(0/1/0)
MLC1	megalencephalic leukoencephalopathy with subcortical cysts 1	22q13.33	5(1/4/0)

SNPs in LD with rs137931 (count: 0) View in gBrowse (chr22:50085822..50085821 )

Overlap with SZ from cross-disorder studies (count: 1)

Reference	Statistical Result	Description	Result Category
Severinsen, J. E., 2006 (b)	P-value = 0.844 in SZ, P-value = 0.5796 in BD and SZ		Negative

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