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)