| Disease |
Gene |
OMIM |
Mutation |
| ACUTE MYOCARDIAL INFARCTION |
LTA
(LYMPHOTOXIN ALPHA, TUMOR NECROSIS FACTOR BETA TNFB)
|
153440 |
A252G
C804A
|
| ALZHEIMER DISEASE |
APOE
(APOLIPOPROTEIN E) |
107741 |
E2,
E3, E4 Genotype |
| ALZHEIMER DISEASE |
ALPHA-2 MACROGLOBULIN (A2M) |
103950 |
V1000I
|
| ALZHEIMER DISEASE |
BUTYRYLCHOLINESTERASE (BCHE, K-VARIANT) |
177400
|
A539T
|
| ALZHEIMER DISEASE |
CATHEPSIN D (CTSD) |
116840
|
A224V
|
| ALZHEIMER DISEASE |
CYSTATIN C (CYSTATIN 3, CST3) |
604312
|
A25T
|
| ALZHEIMER DISEASE |
LIPOPROTEIN LIPASE GENE (LPL) |
238600
|
N291S
|
| ALZHEIMER DISEASE |
LIPOPROTEIN RECEPTOR-RELATED PROTEIN (LRP) |
107770
|
C766T
|
| ALZHEIMER DISEASE |
MYELOPEROXIDASE (MPO) |
606989
|
-463G>A
|
| CARDIAC RISK |
AGT
(ANGIOTENSIN I) |
106150 |
M235T
|
CELIAC DISEASE
» GLUTEN ENTEROPATHY
|
DQA1
DQB1
DRB1 |
212750 |
*0501
*0201
*04 |
| CORONARY HEART DISEASE |
APOE
(APOLIPOPROTEIN E) |
107741 |
E2,
E3, E4 Genotype |
| CORONARY SPASM |
NOS3
(ENOS, ENDOTHELIAL NITROGEN - MONOXIDE SYNTHASE 3) |
163729 |
G894T
(E298D) |
CROHN DISEASE
» INFLAMMATORY BOWEL
DISEASE 1, IBD1 |
CARD15
(NOD2) |
605956 |
R702W,
G908R, 1007fs |
| DEEP VENOUS
TROMBOSIS |
FACTOR 5 (LEIDEN) |
227400 |
G1691A |
| DEEP VENOUS
TROMBOSIS |
FACTOR 2 |
176930 |
G20210A |
| DEEP VENOUS TROMBOSIS |
ANTITHROMBOTIC PANEL (FACTOR 2 and FACTOR 5) |
. |
. |
| DEEP VENOUS TROMBOSIS |
METHYLENE TETRA HYDRO FOLATE REDUCTASE (MTHFR) |
607093 |
A1298C |
| DEEP VENOUS
TROMBOSIS |
METHYLENE TETRA HYDRO FOLATE REDUCTASE (MTHFR) |
607093 |
C677T |
| DEEP VENOUS
TROMBOSIS |
PLASMINOGEN ACTIVATOR INHIBITOR (PAI1) |
173360 |
Del/Ins, 4G/5G |
| DEEP VENOUS
TROMBOSIS |
ANGIOTENSIN CONVERTING ENZYME (ACE) |
106180 |
Ins/del |
| DEEP VENOUS
TROMBOSIS |
FACTOR 13 |
134570 |
Val34Leu |
| DEEP VENOUS
TROMBOSIS |
ANTITHROMBOTIC PANEL
(FACTOR 5, FACTOR 2, MTHFR)
|
|
4
Mutations: G1691A, G20210A, C677T, A1298C |
| HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV, AIDS),
SUSCEPTIBILITY TO |
CCR5
(CHEMOKINE, CC MOTIF, RECEPTOR 5) |
601373 |
32-bp
Deletion |
| HYPERTENSION |
NOS3
(ENOS, ENDOTHELIAL NITROGEN - MONOXIDE SYNTHASE 3) |
163729 |
G894T
(E298D) |
| HYPERTENSION |
ACE
(ANGIOTENSIN 1-CONVERTING ENZYME) |
163729 |
Ins/del |
LACTASE DEFICIENCY
» LACTOSE
INTOLERANCE
|
LCT
(LACTASE) |
603202 |
C13910T |
| OSTEOPOROSIS |
COL1A1 |
120150 |
IVS1,
2046G-T |
| OSTEOPOROSIS |
VDR
(VITAMIN D RECEPTOR, 1,25-DIHYDROXYVITAMIN D3 RECEPTOR) |
601769 |
start
codon polymorphism |
PERIDONTITIS
|
IL1A
(INTERLEUKIN 1-ALPHA)
IL1B (INTERLEUKIN 1-BETA) |
147760
147720 |
IL1A-889
IL1B+3953 |
| RHEUMATOID ARTHRITIS |
SLC22A4 |
604190 |
INTRON
1 SNP |
| SPORTS PERFORMANCE |
ACTN3
(ACTININ, ALPHA-3) |
102574 |
R577X |
| THROMBOPHILIA |
HABP2
(HYALURONAN-BINDING PROTEIN 2,FACTOR VII-ACTIVATING PROTEASE,
FSAP) |
603924 |
Whole
Gene |
