Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11191419
rs11191419
BORCS7 ; BORCS7-ASMT
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.710 GeneticVariation BEFREE We, therefore, used highly sensitive measures of allele-specific expression to assess cis-regulatory effects associated with the two best-supported schizophrenia risk variants (SNP rs11191419 and indel ch10_104957618_I/rs202213518) on the primary positional candidates BORCS7, AS3MT, CNNM2, and NT5C2 in the human brain. 27004590

2016