Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057524157
rs1057524157
DEAF1
T 0.700 GeneticVariation CLINVAR Exome analysis of Smith-Magenis-like syndrome cohort identifies de novo likely pathogenic variants. 28213671

2017
dbSNP: rs1057524157
rs1057524157
DEAF1
T 0.700 GeneticVariation CLINVAR Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype. 28940898

2017
dbSNP: rs1554944271
rs1554944271
DEAF1
G 0.700 GeneticVariation CLINVAR Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype. 28940898

2017
dbSNP: rs2148710
rs2148710
FYN
T 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs2844775
rs2844775
TRIM26
A 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs3752433
rs3752433
PHEX ; PTCHD1-AS
A 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs6954895
rs6954895 		G 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884

2014
dbSNP: rs1057518644
rs1057518644
HGSNAT
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503383
rs1060503383
SYNGAP1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131691771
rs1131691771
PHIP ; IRAK1BP1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs142239530
rs142239530
STIM1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554210073
rs1554210073
PHIP
A 0.700 CausalMutation CLINVAR

dbSNP: rs1558373252
rs1558373252
SOX11 ; LINC01248
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562127631
rs1562127631
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1562134961
rs1562134961
PHIP ; IRAK1BP1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1562150844
rs1562150844
PHIP
C 0.700 CausalMutation CLINVAR

dbSNP: rs1568019012
rs1568019012
LAMA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs370717845
rs370717845
HGSNAT
A 0.700 CausalMutation CLINVAR

dbSNP: rs80338945
rs80338945
GJB2
G 0.700 CausalMutation CLINVAR

dbSNP: rs80358284
rs80358284
FZD4 ; PRSS23
C 0.700 CausalMutation CLINVAR

dbSNP: rs866294686
rs866294686
TRIM8 ; LOC105378460
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886041116
rs886041116
ADNP
A 0.700 GeneticVariation CLINVAR