Critical Genetics Basic
NutraHacker reports mutations in your raw DNA data that have been identified as being critically important.
The conditions examined in this report include:
- 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
- ACVRL1
- APC
- BRCA1
- BRCA2
- BTD
- CACNA1S
- COL3A1
- FBN1
- GAA
- HFE
- HNF1A
- MSH2
- MSH6
- MUTYH
- OTC
- PCSK9
- RET
- RYR1
- SCN5A
- SDHAF2
- STK11
- TGFBR2
- TP53
- VHL
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