SNP Report

Basic Info

Name	rs112896133 dbSNP Ensembl
Location	chr19:12318968 - 12318968(1)
Variant Alleles	G/A
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.00239617
Functional Annotation	downstream_gene_variant; stop_gained.
Consequence to Transcript	downstream_gene_variant(ENST00000594577, ENST00000595977, ENST00000601858); stop_gained(ENST00000293725)
No. of Studies	1 (Positive: 0; Negative: 0; Trend: 1)
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
Georgi, B., 2014	G/A		7 in BPI, 8 in Well 7 in BPI, 8 in Well	Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. More...	Trend

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
ZNF563	zinc finger protein 563	19p13.2	1(0/0/1)

SNPs in LD with rs112896133 (count: 0) View in gBrowse (chr19:12318968..12318968 )

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

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