PCR

  • rs28969505
  • APOE4
  • rs5882
  • APOE4
  • rs1042522
  • rs1800795
  • rs1800896
  • rs2542052
  • APOE polymorphism
  • rs4646994
  • rs1801133
  • SI000565Q
  • rs4646
  • rs2234693
  • rs9536314
  • rs1800871
  • IL6 VNTR A/B/C/D
  • Cdx2–GATA haplotypes
  • G477T
  • rs1800896
  • rs72533289
  • rs2866164
  • rs1801274
  • rs4646994
  • APOE polymorphism
  • rs282070
  • rs2111699
  • rs1799945
  • rs1801133
  • rs2866164
  • rs662
  • rs854560
  • 192/55 loci
  • CYP2D6*3
  • CYP2D6*4
  • GSTM1 deletion
  • NAT2*5A (C 481 T), NAT2*6A (G 590 A), NAT2*7A (G 857 A), and NAT2*14A (G 191 A)
  • rs11039149
  • rs189037
  • microsatellite polymorphism surrounded by rs2288377, rs5742612, and rs35767
  • STR variation
  • codon 192
  • codon 55
  • length (STR polymorphism)
  • (HLA)-A1, B8, DR3
  • rs1800629
  • rs909253
  • rs429358 + rs7412
  • rs4340
  • rs1800629
  • rs1800896 - rs1800629
  • GH1 "intron SNP"
  • rs4646994
  • rs2234693 - rs2234693
  • rs9340799
  • APOE haplotype - rs1346044
  • APOE polymorphism
  • rs3087425
  • rs1801195
  • rs1346044
  • rs11279109
  • SI000565Q
  • SI000565Q
  • rs11279109 - APOB XbaI
  • APOB XbaI − SI000565Q
  • rs11279109 - SI000565Q
  • rs11279109 - APOB XbaI - SI000565Q
  • APOE polymorphism - HP1/2 common polymorphism
  • HP1/2 common polymorphism
  • rs1800795
  • E4
  • rs1800562
  • rs1799945
  • rs1800730
  • (A/C)−110
  • rs1800795 + (rs429358, rs7412)
  • KL-VS
  • DRB1/DQB1
  • rs2229765
  • A-3826G (rs1800592) - C-3740A
  • rs1800592
  • C-3740A
  • rs73598374
  • rs1800629
  • rs361525
  • rs6166
  • rs1801282
  • rs1042522
  • -
  • rs1800896
  • mt5178A
  • rs429358, rs7412
  • rs1801133
  • -
  • rs4880
  • -
  • A/G
  • -
  • -
  • -
  • -
  • rs429358, rs7412
  • rs28969505
  • rs189037 (genotype)
  • -
  • -
  • rs675
  • rs5110
  • rs2234669
  • rs1800471
  • rs1800470
  • rs1800469
  • rs1800468
  • rs429358, rs7412
  • rs2075650
  • rs693
  • rs1042031
  • S61712.1 (GenBank, 3` VNTR)
  • intron 10, VNTR (50 bp)
  • rs9536314
  • rs2430561
  • -
  • VNTR
  • HUMREN4 (STR)
  • HUMTHO1 (STR)
  • (GT)n (exon1)
  • rs4880
  • 3'APOB-VNTR
  • HLA-DQA polymorphisms
  • HLA-DQB polymorphisms
  • rs2229765
  • rs146205520
  • rs361072
  • rs1801278
  • T/C +97347
  • rs1805081
  • rs1631685
  • rs1788799
  • -
  • HUMTHO1 (STR), haplogroups
  • rs9282861
  • rs1764391
  • rs952706
  • rs5882
  • rs662
  • rs2542052
  • rs2866164
  • rs429358, rs7412
  • -
  • rs1800795
  • -
  • rs1061170
  • -
  • rs3758391
  • rs4746720
  • rs854560
  • rs662
  • rs4646994
  • rs2542052
  • rs2542052
  • BF
  • -107 C/T
  • rs73598374

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