Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562846694
rs1562846694
TFR2 ; ACTL6B
G 0.700 GeneticVariation CLINVAR Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination. 31134736

2019
dbSNP: rs11655081
rs11655081
ARSG
0.700 GeneticVariation GWASCAT Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus? 24375517

2014
dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1564045331
rs1564045331
XPA
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568925507
rs1568925507
KCNQ2
TCTTCTCAAAGTGCTTCTGCCTGTGCTGCTCCTGAAC 0.700 CausalMutation CLINVAR

dbSNP: rs587784347
rs587784347
PLA2G6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs752746786
rs752746786
GNB1
G 0.700 CausalMutation CLINVAR

dbSNP: rs773171451
rs773171451
KCNQ2 ; LOC105372724
A 0.700 GeneticVariation CLINVAR

dbSNP: rs778543124
rs778543124
XPA
A 0.700 CausalMutation CLINVAR