Gene | Gene or Chromosomal area was implicated in: | Variation | Polymorphism was implicated in: |
---|---|---|---|
ADRB2 5q32-34 | • Susceptibility to DM2 [26], also in interaction with chromosome 10q23.3 [27]. | Gln27Glu | • Independent contributor in the development of type 2 DM [28] |
CBS 21q22.3 | • Hyperhomocysteinemia [16] which, in turn, is related to diabetic nephropathy [17]. | Ile278Thr | • Homocysteinuria [18]. |
APOA4 11q23 | • Contained in the same region as Apo C-III | Thr347Ser | • Plasma glucose in women [24]. |
APOC3 11q23 | • Well-known diabetes region [21]. | C1100T |  |
 | • APOC3(C-482T) was associated with fasting insulin [22] and in interaction with LIPC -514 C>T also on glucose tolerance [23] |  |  |
APOB 2p24 |  | Thr71Ile | • Interaction between ApoB(Thr71Ile and glucose tolerance on lipid parameters [19] |
GNB3 12p13 | • Age-of-onset of DM2 [29]. | C825T | • Implicated as independent contributor in development of DM2 [30] |
 |  |  | • Insulin resistance [31]. |
 |  |  | • Insulin-mediated vasodilation [32]. |
APOB 2p24 |  | Thr71Ile | • Interaction between ApoB(Thr71Ile and glucose tolerance on lipid parameters [19] |
CETP 16q21 | • CETP (Intron 1 TaqIB +/-) appeared to help significantly in identification of DM2 [33] | Ile405Val |  |
 | • In our present study, CETP (Intron Taq1B+/-) was in LD with a.o. CETP(C-630A) and (Ile405Val). |  |  |
SELE 1q23-25 | • Chromosomal area was implicated in the metabolic syndrome [34]. | Leu554Phe |  |
ITGA2 5q23-31 | • The ITGA2 C807T polymorphism may be associated with an increased risk of diabetic retinopathy [35] | G873A | • Risk factor for retinal vein occlusion [36]. |