I recently had my DNA tested and I think it's something every cruiser should have done before making long range plans.
I've discovered that I don't carry the APOE4 gene for Alzheimer's or any of the considerable number of other known genetic diseases in the 23andme database and can make long term plans with reasonable confidence.
https://www.23andme.com/you/health/drug_response/
They also test for your likely responses to certain drugs and which drugs will
work or not.
I'm going to copy/paste some of what I've received from 23andme so you can see how helpful this can be. I don't have any financial interest in the company, just a satisfied customer.
Unfortunately, the graph gets screwed up when I post it here but here is a list of some of the diseases tested.
Name Confidence Status
Alpha-1 Antitrypsin Deficiency
Variant Absent
Agenesis of the Corpus Callosum with Peripheral Neuropathy (ACCPN)
Variant Absent
Autosomal Recessive Polycystic Kidney Disease
Variant Absent
ARSACS
Variant Absent
Beta Thalassemia
Variant Absent
Bloom's Syndrome
Variant Absent
BRCA Cancer Mutations (Selected)
Variant Absent
Canavan Disease
Variant Absent
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
Variant Absent
Cystic Fibrosis
Variant Absent
D-Bifunctional Protein Deficiency
Variant Absent
Dihydrolipoamide Dehydrogenase Deficiency
Variant Absent
DPD Deficiency
Variant Absent
Familial Dysautonomia
Variant Absent
Factor XI Deficiency
Variant Absent
Fanconi Anemia (FANCC-related)
Variant Absent
Familial Hypercholesterolemia Type B
Variant Absent
Familial Hyperinsulinism (ABCC8-related)
Variant Absent
Familial
Mediterranean Fever
Variant Absent
G6PD Deficiency
Variant Absent
Gaucher Disease
Variant Absent
GRACILE Syndrome
Variant Absent
Glycogen
Storage Disease Type 1a
Variant Absent
Glycogen
Storage Disease Type 1b
Variant Absent
Hemochromatosis
Variant Absent
Primary Hyperoxaluria Type 2 (PH2)
Variant Absent
Hypertrophic Cardiomyopathy (MYBPC3 25bp-deletion)
Variant Absent
LAMB3-related Junctional Epidermolysis Bullosa
Variant Absent
Limb-girdle Muscular Dystrophy
Variant Absent
Leigh Syndrome, French Canadian Type (LSFC)
Variant Absent
Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency
Variant Absent
Maple Syrup Urine Disease Type 1B
Variant Absent
Mucolipidosis IV
Variant Absent
Neuronal Ceroid Lipofuscinosis (CLN5-related)
Variant Absent
Neuronal Ceroid Lipofuscinosis (PPT1-related)
Variant Absent
Niemann-Pick Disease Type A
Variant Absent
Nijmegen Breakage Syndrome
Variant Absent
Connexin 26-Related Sensorineural Hearing Loss
Variant Absent
Pendred Syndrome
Variant Absent
Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1)
Variant Absent
Salla Disease
Variant Absent
Sickle Cell Anemia & Malaria Resistance
Variant Absent
Tay-Sachs Disease
Variant Absent
Torsion Dystonia
Variant Absent
Tyrosinemia Type I
Variant Absent
Zellweger Syndrome Spectrum
Variant Absent
Phenylketonuria
No Data