Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587783672
rs587783672
T 0.720 CausalMutation CLINVAR

dbSNP: rs193929355
rs193929355
T 0.710 CausalMutation CLINVAR

dbSNP: rs80356625
rs80356625
A 0.710 CausalMutation CLINVAR

dbSNP: rs1057515576
rs1057515576
GAAAA 0.700 CausalMutation CLINVAR

dbSNP: rs1057518903
rs1057518903
A 0.700 CausalMutation CLINVAR

dbSNP: rs1135401784
rs1135401784
CP
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553769428
rs1553769428
HJV
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559279177
rs1559279177
HJV
T 0.700 CausalMutation CLINVAR

dbSNP: rs28936415
rs28936415
A 0.700 GeneticVariation CLINVAR

dbSNP: rs386134141
rs386134141
CP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783669
rs587783669
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587783673
rs587783673
T 0.700 CausalMutation CLINVAR

dbSNP: rs587783675
rs587783675
G 0.700 CausalMutation CLINVAR

dbSNP: rs886040857
rs886040857
A 0.700 CausalMutation CLINVAR

dbSNP: rs74551128
rs74551128
0.010 GeneticVariation BEFREE Fewer patients with the A455E mutation had pancreatic insufficiency (21.2 percent vs. 93.9 percent, P < 0.001), and none had diabetes mellitus (0 percent vs. 27.3 percent, P = 0.004). 7539891

1995

dbSNP: rs1801483
rs1801483
0.020 GeneticVariation BEFREE A mutation in the glucagon receptor gene (Gly40Ser): heterogeneity in the association with diabetes mellitus. 7589886

1995

dbSNP: rs4994
rs4994
0.050 GeneticVariation BEFREE A tryptophan to arginine (Trp64Arg) mutation in the beta 3-adrenergic receptor (beta 3-AR) gene has been implicated in diabetes and obesity. 8826971

1996

dbSNP: rs1255911887
rs1255911887
0.010 GeneticVariation BEFREE Glucokinase instability, not low enzyme catalytic activity, may be the cause of diabetes mellitus with E70K and E300K mutants. 9078243

1997

dbSNP: rs33929415
rs33929415
HBB
0.010 GeneticVariation BEFREE Hemoglobin Old Dominion/Burton-upon-Trent, beta 143 (H21) His-->Tyr, codon 143 CAC-->TAC--a variant with altered oxygen affinity that compromises measurement of glycated hemoglobin in diabetes mellitus: structure, function, and DNA sequence. 9559035

1998

dbSNP: rs1444739794
rs1444739794
GCK
0.010 GeneticVariation BEFREE The V62A mutation, which has not been previously reported, cosegregated with diabetes in the N2 family. 9736233

1998

dbSNP: rs1801282
rs1801282
0.100 GeneticVariation BEFREE Pro12Ala missense mutation of the peroxisome proliferator activated receptor gamma and diabetes mellitus. 9918859

1999

dbSNP: rs1805192
rs1805192
0.100 GeneticVariation BEFREE Pro12Ala missense mutation of the peroxisome proliferator activated receptor gamma and diabetes mellitus. 9918859

1999

dbSNP: rs1267969615
rs1267969615
ACE
0.070 GeneticVariation BEFREE Relative nocturnal systolic and diastolic pressures in patients with diabetes were higher than in healthy age- and height-matched controls; no association was found with the angiotensinogen gene M235T polymorphism. 9950302

1999

dbSNP: rs699
rs699
AGT
0.070 GeneticVariation BEFREE Relative nocturnal systolic and diastolic pressures in patients with diabetes were higher than in healthy age- and height-matched controls; no association was found with the angiotensinogen gene M235T polymorphism. 9950302

1999

dbSNP: rs1267969615
rs1267969615
ACE
0.070 GeneticVariation BEFREE We examined angiotensin-converting enzyme (ACE) DD/II and angiotensinogen (Atg) M235T polymorphism in a cohort of Chinese patients with type II diabetes with an average duration of diabetes of 14 years. 10352194

1999