Mikilvæg Erfðafræði Grunnur

NutraHacker greinir stökkbreytingar í hráum DNA gögnum þínum sem hafa verið auðkenndar sem mikilvægar.

Aðstæðurnar sem skoðaðar eru í þessari skýrslu innihalda:

• Biotinidase deficiency
• Ehlers-Danlos syndrome, vascular type
• Familial adenomatous polyposis
• Familial hypercholesterolemia
• Hereditary breast and ovarian cancer
• Hereditary hemochromatosis
• Hereditary hemorrhagic telangiectasia
• Hereditary paraganglioma-pheochromocytoma syndrome
• Li-Fraumeni syndrome
• Lynch syndrome
• Malignant hyperthermia susceptibility
• Marfan syndrome, Loeys-Dietz syndromes, and familial thoracic aortic aneurysms and dissections
• Maturity-onset diabetes of the young
• Multiple endocrine neoplasia type 2
• MYH-associated polyposis; adenomas, multiple colorectal, FAP type 2; colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas
• Ornithine transcarbamylase deficiency
• Peutz-Jeghers syndrome
• Pompe Disease
• Romano-Ward long-QT syndrome types 1, 2, and 3, Brugada syndrome
• Von Hippel–Lindau syndrome

Genin sem skoðuð eru í þessari skýrslu innihalda:

• ACVRL1
• APC
• BRCA1
• BRCA2
• BTD
• CACNA1S
• COL3A1
• FBN1
• GAA
• HFE
• HNF1A
• MSH2
• MSH6
• MUTYH
• OTC
• PCSK9
• RET
• RYR1
• SCN5A
• SDHAF2
• STK11
• TGFBR2
• TP53
• VHL

Fyrir sýnishorn skýrslu smelltu hér

Hlaða upp hráum DNA gögnum til að byrja með ókeypis DNA hráa gagnagreiningu þína í dag!