Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1135402761
rs1135402761
SYT1
C 0.700 CausalMutation CLINVAR

dbSNP: rs137852695
rs137852695
PPT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs143657539
rs143657539
PPT1
T 0.700 CausalMutation CLINVAR

dbSNP: rs144900171
rs144900171
SYT1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554504663
rs1554504663
RHOBTB2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555119899
rs1555119899
ATM ; C11orf65
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1565922388
rs1565922388
SYT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565922395
rs1565922395
SYT1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565962725
rs1565962725
SYT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs369691608
rs369691608
BCS1L ; ZNF142
T 0.700 CausalMutation CLINVAR

dbSNP: rs421016
rs421016
GBA
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs886039494
rs886039494
GNAO1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554059320
rs1554059320
RICTOR
G 0.700 GeneticVariation CLINVAR Nutrition education in the medical school curriculum: a proposal for action: a curriculum design. 2006

1976
dbSNP: rs1555605688
rs1555605688
CLTC
T 0.700 GeneticVariation CLINVAR Clathrin: a unique protein associated with intracellular transfer of membrane by coated vesicles. 1063406

1976
dbSNP: rs1553245178
rs1553245178
ATP1A2
A 0.700 CausalMutation CLINVAR A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations. 1361034

1992
dbSNP: rs1554794342
rs1554794342
ERCC6
T 0.700 CausalMutation CLINVAR Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes. 1372469

1992
dbSNP: rs185142838
rs185142838
ERCC6
A 0.700 CausalMutation CLINVAR Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes. 1372469

1992
dbSNP: rs1555050165
rs1555050165
GRIA4
G 0.700 GeneticVariation CLINVAR Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain. 1374769

1992
dbSNP: rs786205232
rs786205232
KCNA2
T 0.700 CausalMutation CLINVAR An essential 'set' of K+ channels conserved in flies, mice and humans. 1377421

1992
dbSNP: rs886041761
rs886041761
KCNA2
T 0.700 GeneticVariation CLINVAR An essential 'set' of K+ channels conserved in flies, mice and humans. 1377421

1992
dbSNP: rs1557082399
rs1557082399
ATRX
T 0.700 CausalMutation CLINVAR X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis. 1415255

1992
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. 1423634

1992
dbSNP: rs1131691712
rs1131691712
CACNA1A
GA 0.700 CausalMutation CLINVAR Familial paroxysmal ataxia: report of a family. 1564484

1992
dbSNP: rs1553732126
rs1553732126
ADCY5
CG 0.700 GeneticVariation CLINVAR Isolation and characterization of a novel cardiac adenylylcyclase cDNA. 1618857

1992