Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13176113
rs13176113 		0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs13187934
rs13187934 		0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs1346536
rs1346536 		0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs1408744
rs1408744 		0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs14135
rs14135
MACROD2 ; MACROD2-AS1
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs1429793
rs1429793
NELL1 ; LOC105376585
0.700 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
dbSNP: rs1475531
rs1475531
MACROD2 ; MACROD2-AS1
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs1555144459
rs1555144459
PKP2
CA 0.700 GeneticVariation CLINVAR Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2. 16549640

2006
dbSNP: rs1555144459
rs1555144459
PKP2
CA 0.700 GeneticVariation CLINVAR Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. 15489853

2004
dbSNP: rs1555144459
rs1555144459
PKP2
CA 0.700 GeneticVariation CLINVAR Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations. 22781308

2012
dbSNP: rs1555453538
rs1555453538
POLG ; MIR6766
C 0.700 GeneticVariation CLINVAR Polymerase gamma 1 mutations: clinical correlations. 20220442

2010
dbSNP: rs1555453538
rs1555453538
POLG ; MIR6766
C 0.700 GeneticVariation CLINVAR Clinical and molecular features of POLG-related mitochondrial disease. 23545419

2013
dbSNP: rs1555453538
rs1555453538
POLG ; MIR6766
C 0.700 GeneticVariation CLINVAR Understanding the Epilepsy in POLG Related Disease. 28837072

2017
dbSNP: rs1555640521
rs1555640521
LAMA1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1558373252
rs1558373252
SOX11 ; LINC01248
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1562171209
rs1562171209
PHIP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1563183492
rs1563183492
AUTS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1566823361
rs1566823361
FGF14
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1567941252
rs1567941252
PCGF2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568507354
rs1568507354
RYR1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569525894
rs1569525894
SLC9A6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs16919315
rs16919315
TMEM132B
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs17007739
rs17007739 		0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs17134117
rs17134117
SDK1
0.700 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
dbSNP: rs1718101
rs1718101
CNTNAP2
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012