Gene: RELN ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1275980031
rs1275980031
RELN
0.010 GeneticVariation BEFREE The de novo autism spectrum disorder RELN R2290C mutation reduces Reelin secretion and increases protein disulfide isomerase expression. 28419454

2017
dbSNP: rs7341475
rs7341475
RELN
0.010 GeneticVariation BEFREE We found that RELN rs736707 was significantly related with psychiatric disorders (schizophrenia, autism spectrum disorders and attention-deficit hyperactivity disorder) in Asian group (C vs T, OR=1.26, 95% CI=1.13-1.41, P<0.01, FDR<0.01), and rs7341475 was only significantly associated with reduced risk of schizophrenia in Caucasian (A vs G, OR=0.88, 95% CI=0.82-0.95, P<0.01, FDR<0.01). 28506622

2017
dbSNP: rs362691
rs362691
RELN
0.010 GeneticVariation BEFREE Odds ratios (ORs) with 95% confidence intervals were used to estimate the associations between three RELN variants (rs736707, rs362691</span>, and GGC repeat variant) and ASD. 24453138

2014
dbSNP: rs736707
rs736707
RELN ; LOC101927870
0.010 GeneticVariation BEFREE Odds ratios (ORs) with 95% confidence intervals were used to estimate the associations between three RELN variants (rs736707, rs362691, and GGC repeat variant) and ASD. 24453138

2014