On 1 I look for various cancers
On 2 for pulmonary hypertension
On 3 for cataracts and diabetes
On 4 for hemophilia and Huntington’s
On 5 for Parkinson’s
On 6 for celiac disease
On 7 for fibrosis
On 8 for hypothyroidism
On 9 for ataxia
On 10 for leukemia
On 11 for sickle cell
On 12 for Parkinson’s
On 13 for retinoblastoma
On 14 for Marfan syndrome
On 15 for Tay-Sach’s
On 16 for Chron’s
On 17 for deafness
On 18 for Alzheimer’s
On 19 for breast cancer
etc etc
Since I know whereto look, and what to look for, and I have the full male Genome, and the full female Genome, I can see where there’s a + and a +.
When this happens along the 1822 genes on my template, I can put a point score on it based on the seriousness of the defect and what + + is likely to mean for that gene.
For some + + will mean sure expression.
For some it depends on dominance or not.
For those with a + and a – it depends on which side has the +.
Anyhow my machine has all that in its algorithm for points adding up.
It just goes down the line 1822 gene places, and adds up the total risk score.
The risk score will make one light illuminate and it will be red, orange, yellow blue, or green.
The prospective mating pair get the see the light.
What they do with the info is none of my business.
They may choose to go ahead, and mate. Of they may decide not to do that.
Their decision. Not mine.
Truth is a good thing. It helps decisions be better.
My machine will do in 1 second for $1000 something you can get done in only 2 years for only $50,000 from a Geneticist with degrees on the wall and a white lab coat.
You say you want that? OK — get what you want.
I give you options.
You make your decisions.
Not my worry.
Do as you like.
The Better Babies Patent Entails 1822 Relevant Genes. I look on the Various Chromosomes
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