Selectively breeding Jews to turn them into goblins

imagine how good this punishment would be.
taking a race of people who have caused suffering for thousands of years into a race of mongrelized humiliating short green shekel goblins?. ofcourse this would require many years of selective breeding and heavy gene editing
but i think this would ad a sort of divine comedy to the end of Jews as a species

Attached: cheddar goblin.jpg (320x320, 24K)

"Homo-Cabalos" or "Visionary Hebrews"

>to turn them into goblins
uhhh....

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no imagine seeing these things irl it wouldn't be nice

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turning them into the exact stereotype and thing they are with a bigger punishment added to it, whites split the atom to fight nonwhites, the Japanese. now it is time for us to crack into gene editing to destroy Jewish genetic makeup so bad they couldn't be recognized to pay for the endless suffering they have caused

tf are you talking about, have you never seen a jew? that's where they got goblins from dumbass

we are talking about complete genetic lobotomization, an complete attack on their fucking genes. all tomorrows style

i'd rather just exterminate them, they're already satan spawn that has to take our blood to keep their genetics from breaking down after three generations so I'd say their genes are already pretty fucked m8

because of their greed they already done it to themselves

>The genetics of Ashkenazi Jews have been particularly well-studied, resulting in the discovery of many genetic disorders associated with this ethnic group.

Ashkenazi Jewish Diseases
3-Phosphoglycerate Dehydrogenase Deficiency
Abetalipoproteinemia
Alport Syndrome
Arthrogryposis, Mental Retardation and Seizures
Bardet-Biedl Syndrome
Bloom Syndrome
Canavan Disease
Carnitine Palmitoyltransferase ll Deficiency
Choreoacanthocytosis
Congenital Amegakaryocytic Thrombocytopenia
Congenital Disorder of Glycosylation la
Cystic Fibrosis
Deafness-Autosomal Recessive 77
Dyskeratosis Congenita, Autosomal Recessive
Ehlers-Danlos VllC
Enhanced S-Cone Syndrome
Factor XI Deficiency
Familial Dysautonomia
Familial Hypercholesterolemia
Familial Hyperinsulinism
Familial Mediterranean Fever
Fanconi Anemia-Group C
Fragile X Syndrome
Galactosemia
Gaucher Disease
Glycogen Storage Disease 1A
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IV / Adult Polyglucosan Body Disease
Glycogen Storage Disease Type VII
Hermansky-Pudlak Syndrome 3
Joubert Syndrome 2
Lipoamide Dehydrogenase Deficiency
Maple Syrup Urine Disease 1B
Mitochondrial Complex 1 Deficiency
Mucolipidosis IV (ML4)
Multiple Sulphatase Deficiency
Nemaline Myopathy 2
Niemann-Pick Disease Type A/B
Nonsyndromic Hearing Loss
Osteopetrosis 1
Phenylalanine Hydroxylase Deficiency
Polycystic Kidney Disease, Autosomal Recessive
Pontocerebellar Hypoplasia Type 1A
Primary Ciliary Dyskinesia DNAH5
Primary Ciliary Dyskinesia DNAI1
Primary Ciliary Dyskinesia DNAI2
Primary Hyperoxaluria Type 3
Retinitis Pigmentosa 28
Retinitis Pigmentosa 59
Smith-Lemli-Opitz Syndrome
Spinal Muscular Atrophy
Tay-Sachs Disease
Tyrosinemia-Type 1
Usher Syndrome-Type IF
Usher Syndrome-Type III
Walker Warburg Syndrome and Other FKTN-Related Dystrophies
Wilson Disease
Zellweger Syndrome Spectrum-PEX2

you make me cry :(