
- Genetic abnormalities, technically referred as single nucleotide polymorphisms (SNPs), are commonly called or thought of as ‘genetic mutations,’ in layman’s terms, however this is not a true representation of what SNPs actually are
- A SNP occurs when genetic information is miscopied or mistranslated during RNA translation and results in one nucleotide being different in a strand of DNA
- SNPs occur almost once in every 1,000 nucleotides on average, which yields about 4 to 5 million SNPs in a person’s genome1
- SNPs can range from harmless to having serious or terminal effects on human health
- SNPs that are specifically related to nutrients can either inhibit or promote absorption or production of the nutrient in question
- In order to assess the action of a SNP, it is critical to measure the nutrients associated with that SNP
- Vibrant’s NutriPro panel is a test to measure levels of various genetic mutations present in an individual’s body along with the measure of the actual nutrient value in order to display where the deficiency or excess is occurring
- Testing for the presence of nutritional SNPs can give a complete picture of the predispositions to various nutrient deficiencies along with the current levels of these nutrients and aid practitioners In designing the most effective interventions for dietary deficiency, genetic disorders, and malabsorptive conditions
- In addition to Vibrant Micronutrients 3.0, also consider ordering Neurotransmitters, Organic Acids, and diagnostic panels such as anemia, lipids, and CBCs
Only healthcare providers licensed in their state may order laboratory testing.
Nutrient
-
Vitamins
- Vitamin A
- Beta carotene
- Vitamin B1
- Vitamin B2
- Vitamin B6
- Vitamin B7
- Vitamin B9
- Vitamin B12
- Vitamin C
- Vitamin D, 25-OH
- 1,25-dihydroxyvitamin D
- Vitamin D2 (Ergocalciferol)
- Vitamin D3 (Cholecalciferol)
- Vitamin E (α-tocopherol)
- Vitamin E (γ tocopherol)
- Vitamin K1
-
Minerals
- Sodium
- Zinc
- Molybdenum
- Alpha lipoic acid
- Tetrahydrobiopterin rs5030853 PAH
- Iodine
- Fluoride
- Phosphorus
- Iron
- RBC Omega fatty acids (n3 and n6)
- Manganese
- Calcium
-
Amino Acids
- Glutamine
- Coenzyme Q
- Glutathione
- Methylmalonic acid(MMA)
- Choline
- Carnitine
- Valine
- Isoleucine
- Leucine
- Serine
- Glycine
- Arginine
- Citrulline
- Tryptophan
- Phenylalanine
- Gamma-aminobutyric acid
-
Fatty Acids
- 11-Eicosenoic Acid
- Alpha-Linolenic Acid (ALA)
- Arachidonic Acid
- Docosahexaenoic Acid (DHA)
- Eicosapentaenoic Acid (EPA)
- Gamma Linolenic Acid (GLA)
- Linoleic acid
rs ID
- rs11645428
- rs7501331, rs12934922
- rs6564851
- rs1667255
- rs11645428
- rs17514104
- rs1799983
- rs778479139
- rs121964972, rs5742905
- rs13078881
- rs1801133, rs1801131
- rs602662, rs492602
- rs526934
- rs33972313
- rs6139591
- rs4257763
- rs6596473
- rs7041, rs4588
- rs12785878
- rs10741657
- rs2282679
- rs4588
- rs10766197, rs1993116
- rs10877012
- rs3782130
- rs12272004
- rs671
- rs2108622
- rs2304478, rs7204044
- rs13266634
- rs11126936
- rs1050450, rs1050450
- rs3877899
- rs594445
- rs12095080
- rs5030853
- rs8007267
- rs225014
- rs4284505
- rs4074995
- rs855791, rs4820268
- rs3811647
- rs1800562, rs1799945
- rs174547, rs174537
- rs13107325
- rs1776029
- rs4516035
- rs6323
- rs3829289, rs3812778
- rs775607037, rs786204770
- rs121909307
- rs1695
- rs291466
- rs121918252
- rs3733890
- rs7946
- rs80356779
- rs1440581
- rs7678928
- rs1440581
- rs2236225
- rs715
- rs7860909
- rs7860909
- rs10488682
- rs5030853
- rs4263535
- rs80356779
- rs174545, rs174561, rs174537
- rs174583
- rs174570, rs174546
- rs174602, rs3734398, rs2236212, rs953413
- rs3734398, rs2236212, rs953413
- rs174579, rs174593, rs174626
- rs174547
Mutated Gene
- BCMO1
- BCO1
- BCMO1
- TTR
- BCMO1
- SLC35F3
- NOS3
- SLC52A3
- CBS
- BTD
- MTHFR
- FUT2
- TCN1
- SLC23A1
- SVCT1, SVCT2
- SVCT1
- SLC23A1
- GC
- NADSYN1
- CYP2R1
- GC
- VDR
- CYP2R1
- CYP27B1
- CYP27B1
- APOA5
- APOA4
- CYP4F2
- SLC12A3
- SLC30A8
- SLC12A3
- GPX1
- SEPP1
- MOCOS
- DIO1
- PAH
- GCH1
- DIO2
- ESR1
- GS14
- TMPRSS6
- TF
- HFE
- FADS1
- SLC39A8
- SLC30A10
- VDR
- MAOA
- SLC1A2
- COQ4
- GSS
- GSTP1
- HICBH
- MUT
- BHMT
- PEMT
- CPT1A
- PPM1K
- PPM1K
- PPM1K
- MTHFD1
- CPS1
- ASS1
- ASS1
- TPH1
- PAH
- GABRA1
- CPT1A
- FADS1
- FADS2
- FADS1
- FADS2
- FADS1
- FADS2
- FADS2
Conditions and Symptoms Associated with Nutritional Genetic Abnormalities Include:
- Nutrient malabsorption
- Nutrient deficiencies
- Nutrient excesses
- Mood disorders
- Cardiometabolic disorders
- Anemia
- Bone-related disorders
- Neurological and mood disorders
- Age-related disorders
- Inflammatory disorders
Will this test tell me if a genetic mutation is being expressed?
Genetic abnormalities, technically referred as single nucleotide polymorphisms (SNPs), are commonly called or thought of as ‘genetic mutations,’ in layman’s terms, however this is not a true representation of what SNPs actually are.
A SNP occurs when genetic information is miscopied or mistranslated during RNA translation and results in one nucleotide being different in a strand of DNA. While this panel does not measure genetic expression, the presence of a SNP alongside the measured nutrient levels in serum, or inside of white or red blood cells, can help your healthcare provider determine if the SNP is contributing to a deficiency or excess of a nutrient.
Recommended Tests to Consider