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ONLINE SERVICE

Analysis of Results of Pharmacogenetic Testing


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This service allows to assume the activity of individual isoenzymes, based on the data on the patient's response to the effects of drugs that he had previously taken. The service provides a list of drugs that can be prescribed to a patient in a standard dose and whose risk of developing unwanted reactions and pharmacoresistance will be minimal. But at the start, choose your organization, groups of drugs, insert the information about the patient and after these choose the drug and the event.






Remember: If you don't know the genotype - do not change it (normal genotype is default)! If you need a help - info@pgx2.com

Nucleotide Change Allele Variant rs Genotype Include in Report
-3860G>A *1C rs2069514
-163C>A *1F rs762551
-729C>T *1K rs12720461
1042G>A *3 rs56276455
1156A>G *4 rs72547516
1291C>T *6 rs28399424
1253+1G>A *7 rs56107638
Nucleotide Change Allele Variant rs Genotype Include in Report
430C>T *2 rs1799853
1075A>C *3 rs1057910
1076T>C *4 rs56165452
1080C>G *5 rs28371686
817delA *6 rs9332131
55C>A *7 rs67807361
449G>A *8 rs7900194
752A>G *9 rs2256871
815A>G *10 rs9332130
1003C>T *11 rs28371685
269T>C *13 rs72558187
485C>A *15 rs72558190
895A>G *16 rs72558192
449G>T *27 rs7900194
Nucleotide Change Allele Variant rs Genotype Include in Report
681G>A *2 rs4244285
276G>C *2B rs17878459
636G>A *3 rs4986893
1A>G *4 rs28399504
1297C>T *5 rs56337013
395G>A *6 rs72552267
819+2T>A *7 rs72558186
358T>C *8 rs41291556
431G>A *9 rs17884712
680C>T *10 rs6413438
-806C>T *17 rs12248560
Nucleotide Change Allele Variant rs Genotype Include in Report
886C>T *2 rs16947
1457G>C *2 rs1135840
408G>C *2A rs1058164
775delA *3 rs35742686
506-1G>A *4 rs3892097
454delT *6 rs5030655
971A>C *7 rs5030867
505G>T/A *8*14 rs5030865
841_843delAAG *9 rs5030656
100C>T *10 rs1065852
181-1G>C *11 rs5030863
124G>A *12 rs5030862
137-138insT->T *15 rs72549357
320C>T *17 rs28371706
1973_1974insG->G *20 rs72549354
1012G>A *29 rs59421388
406G>A *29*70 rs61736512
31G>A *35 rs769258
Sing-dup *36 Gene conversion to CYP2D7 in exon 9
985+39G>A *41 rs28371725
CNV assay *5/XN Del/duplication
Nucleotide Change Allele Variant rs Genotype Include in Report
479T>A *2 rs1801272
1283G>T *5 rs5031017
383G>A *6 rs4986891
1412T>C *7 rs5031016
-48T>G *9 rs28399433
1093G>A *17 rs28399454
1175A>T *18 rs1809810
1427A>G *21 rs6413474
607C>T *23 rs56256500
1312A>T *35 rs143731390
Nucleotide Change Allele Variant rs Genotype Include in Report
785A>G *4 rs2279343
516G>T *6 rs3745274
415A>G *8 rs12721655
136A>G *11 rs35303484
296G>A *12 rs36060847
1172T>A *15 rs35979566
I983T>C *18 rs28399499
-82T>C *22 rs34223104
499C>G *26 rs3826711
Nucleotide Change Allele Variant rs Genotype Include in Report
805A>T *2 rs11572103
416G>A *3 rs11572080
1196A>G *3 rs10509681
792C>G *4 rs1058930
Nucleotide Change Allele Variant rs Genotype Include in Report
227G>A *2 rs72559710
535G>A *4 rs6413419
Nucleotide Change Allele Variant rs Genotype Include in Report
-76G>T *7 rs890293
Nucleotide Change Allele Variant rs Genotype Include in Report
-392G>A *1B rs2740574
1334T>C *3 rs4986910
389G>A *8 rs72552799
1117C>T *12 rs12721629
1247C>T *13 rs4986909
566T>C *17 rs4987161
878T>C *18 rs28371759
522-191C>T *22 rs35599367
Nucleotide Change Allele Variant rs Genotype Include in Report
1193C>A *2 rs28365083
689-1G>A *3 rs776746
58C>T *3A rs28383468
92_93insG->G *3B rs200579169
*14T>C *3 rs15524
624G>A *6 rs10264272
1035_1036insT *7 rs41303343
82C>T *8 rs55817950
1009G>A *9 rs28383479
1337T>C *3K rs41279854
Nucleotide Change Allele Variant rs Genotype Include in Report
34T>G *2 rs3093105
1297G>A *3 rs2108622
Nucleotide Change Allele Variant rs Genotype Include in Report
3730G>A *H7 rs7294
2255C>T *H3 rs2359612
1542G>C *H3 rs8050894
1173C>T *H4 rs9934438
497T>G *H2 rs2884737
-1639G>A *H4 rs9923231
Nucleotide Change Allele Variant rs Genotype Include in Report
521T>C *5 rs4149056
388A>G *1B rs2306283
-910G>A *17 rs4149015
Nucleotide Change Allele Variant rs Genotype Include in Report
3435C>T *6 rs1045642
2677G>T *7 rs2032582
1236C>T *8 rs1128503
Nucleotide Change Allele Variant rs Genotype Include in Report
143A>G *2 rs1229984
1108C>T *3 rs2066702
Nucleotide Change Allele Variant rs Genotype Include in Report
638G>A *2 rs9282861
667G>A *3 rs1801030
Nucleotide Change Allele Variant rs Genotype Include in Report
337T>C *113His rs1051740
416A>G *139Arg rs2234922
Nucleotide Change Allele Variant rs Genotype Include in Report
341T>C *5 rs1801280
590G>A *6 rs1799930
857G>A *7 rs1799931
481C>T *11 rs1799929
803A>G *12 rs1208
282C>T *13 rs1041983
191G>A *14 rs1801279
Nucleotide Change Allele Variant rs Genotype Include in Report
238G>C *2 rs1800462
460A>G *3A*3B rs1800460
719A>G *3A*3C rs1142345
626-1G>A *4 rs1800584
Nucleotide Change Allele Variant rs Genotype Include in Report
313A>G *1B*1C rs1695
341C>T *1C*1D rs1138272
Nucleotide Change Allele Variant rs Genotype Include in Report
293A>G *70G rs1799807
1699G>A *539T rs1803274
Nucleotide Change Allele Variant rs Genotype Include in Report
211G>A *6 rs4148323
Nucleotide Change Allele Variant rs Genotype Include in Report
70C>A *2 rs1799807
142T>G *3 rs2011425
Nucleotide Change Allele Variant rs Genotype Include in Report
19T>G *2 rs6759892
541A>G *2 rs2070959
552A>C *2 rs1105879
Nucleotide Change Allele Variant rs Genotype Include in Report
518C>T *2 rs1042597
Nucleotide Change Allele Variant rs Genotype Include in Report
766G>A *2 rs58597806
Nucleotide Change Allele Variant rs Genotype Include in Report
802C>T *2 rs7439366
Nucleotide Change Allele Variant rs Genotype Include in Report
1905+1G>A *2A rs3918290
1679T>G *13 rs55886062
2846A>T *D949V rs67376798
Nucleotide Change Allele Variant rs Genotype Include in Report
118A>G *2 rs1799971
Nucleotide Change Allele Variant rs Genotype Include in Report
526C>T *2 rs7412
388T>C *4 rs429358
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Psychiatry Cardiology Allergology Oncology




















































(not necessary)

ID
Name of Patient
Date of Birth
Height (cm)
Weight (kg)
Sex (m/w)
Rase (Caucasian/African/Asian)
Electronically Signature Doctors Name






ADDITIONAL

Data Editor


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