MORE Updated DNA REPORTS

What can a lay person like myself interpret FROM jigsaw that is my DNA.

There for I'am ... Doing my research i have found WHEN DNA error occurs you body try's to fix one error but that one fix leads to more.

But how and why CONNECTED as eluded me.

Take one of my inherited conditions or DNA mutations MAPLE SYRUP SYNDROME.

Talks of light chains very bad AND and also was reading about lung health and Light chains.

HOW & WHY Connected.

Here is snap shot of jigsaw that is tad of my DNA errors and mutations.

These reports show your results for specific genetic variants that are associated with a higher risk for developing certain health conditions. However, these reports cannot tell you whether you definitely will, or will not, develop the condition. Note that there are other genetic variants linked to these conditions that are not covered by these reports. Environmental and lifestyle factors can also contribute to these conditions. If any of these conditions run in your family or you think you might have one of these conditions, consult with a healthcare provider about appropriate testing.

NAMECONFIDENCECONFIDENCE

Alpha-1 Antitrypsin Deficiency.

Early-Onset Primary Dystonia (DYT1-TOR1A-Related).

Factor XI Deficiency.

Familial Hypercholesterolemia Type B (APOB-Related).

Familial Transthyretin (TTR) Amyloidosis.

Hereditary Breast and Ovarian Cancer Syndrome (BRCA1- and BRCA2-Related, Selected Mutations).

Hereditary Hemochromatosis (HFE-Related).

Hypertrophic Cardiomyopathy (MYBPC3 25-base-pair Deletion).

Inherited Thrombophilia (Factor V Leiden- and Prothrombin-Related).

Parkinson's Disease (LRRK2- and GBA-Related).

Alzheimer's Disease (APOE Variants).

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Inherited conditions

These reports show your results for specific genetic variants that can cause certain health conditions. Many of these conditions are recessive, meaning that they only occur when you have two variants for that condition, one inherited from each parent. If you have inherited just one variant, you are said to be a "carrier". Carriers usually do not have the condition, but can pass the variant on to their children. Note that these reports cover only a subset of possible variants that may be linked to a condition. It is thus possible to have other variants not covered by these reports.

Agenesis of the Corpus Callosum with Peripheral Neuropathy (ACCPN).

Autosomal Recessive Polycystic Kidney Disease.

Beta Thalassemia.

Bloom's Syndrome.

Canavan Disease

Congenital Disorder of Glycosylation Type 1a (PMM2-CDG).

Connexin 26-Related Sensorineural Hearing Loss.

Cystic Fibrosis.

D-Bifunctional Protein Deficiency.

DPD Deficiency.

Dihydrolipoamide Dehydrogenase Deficiency.

Familial Dysautonom.

Familial Hyperinsulinism (ABCC8-related).

Familial Mediterranean Fever.

Fanconi Anemia (FANCC-related).

G6PD Deficiency.

GRACILE Syndrome.

Gaucher Disease.

Glycogen Storage Disease Type 1a

Glycogen Storage Disease Type 1b

Hereditary Fructose Intolerance.

Junctional Epidermolysis Bullosa (LAMB3-related).

Leigh Syndrome, French Canadian Type (LSFC).

Limb-girdle Muscular Dystrophy

Maple Syrup Urine Disease Type 1B

Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency

Mucolipidosis IV

Neuronal Ceroid Lipofuscinosis (CLN5-related).

Neuronal Ceroid Lipofuscinosis (PPT1-related)

Niemann-Pick Disease Type A

Nijmegen Breakage Syndrome.

Pendred Syndrome.

Primary Hyperoxaluria Type 2 (PH2).

Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1).

Salla Disease.

Sickle Cell Anemia.

Sjögren-Larsson Syndrome.

Tay-Sachs Disease.

Tyrosinemia Type I.

Usher Syndrome Type I (PCDH15-related).

Usher Syndrome Type III.

Zellweger Syndrome Spectrum.

Conclusion is that lot of my genes mutations are from ancestry origans of my dna in world THEN i think as we age our DNA mutates thus pairing mutated genes up.

And thats how i think illness diseases are formed ALSO toxins from work social enviroment we pick must contrabute to dna mutaions pairing.

Well thats what i think GUESS all look at steriodes and what they do to DNA pairs mutations etc.