Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104886033
rs104886033
DHCR7
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518813
rs1057518813
ERCC5 ; BIVM-ERCC5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518907
rs1057518907
GNAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs113993970
rs113993970
HTRA1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121912651
rs121912651
TP53
A 0.700 CausalMutation CLINVAR

dbSNP: rs1345176461
rs1345176461
IRF2BPL ; LOC107984638
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554107200
rs1554107200
HARS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1558027212
rs1558027212
TMCO1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1566823361
rs1566823361
FGF14
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs267606670
rs267606670
ATP1A3
T 0.700 CausalMutation CLINVAR

dbSNP: rs28935468
rs28935468
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs368869806
rs368869806
PTCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs372445155
rs372445155
NPC1
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906686
rs387906686
SCN2A
T 0.700 CausalMutation CLINVAR

dbSNP: rs587777630
rs587777630
STAT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs587784105
rs587784105
NSD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs750331613
rs750331613
GRID2
T 0.700 CausalMutation CLINVAR

dbSNP: rs771063992
rs771063992
DNAJC21
T 0.700 CausalMutation CLINVAR

dbSNP: rs797044849
rs797044849
GRIN2B
G 0.700 GeneticVariation CLINVAR

dbSNP: rs80338903
rs80338903
USH2A
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358257
rs80358257
NPC1
C 0.700 CausalMutation CLINVAR

dbSNP: rs876660634
rs876660634
PTEN
G 0.700 CausalMutation CLINVAR

dbSNP: rs886039469
rs886039469
KCNMA1 ; KCNMA1-AS1
C 0.700 CausalMutation CLINVAR

dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
0.100 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.100 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018