MTHFRSupport Variant Report v2
MTHFRSupport Variant Report Report is intended to translate your results into an easier to understand form. It is not intended to diagnose or treat. For diagnosis or treatment, please present this to yourdoctor (or find a doctor on under "Find a Practitioner"). Additionally, genetic mutations are flags that something could be wrong and not a guarantee thatyou are having all or any of the associated issues. Other factors like environment, ethnic background, diet, age, personal history, etc all have a factor in whether a mutationstarts to present itself or not and when. Copyright 2011-2018 MTHFR Support LLC1/64Liver Detox - Phase I (Figure 1)SNP IDSNP NameRisk AlleleYour AllelesYour Resultsrs1048943CYP1A1*2C A4889GCTT-/-rs1799814CYP1A1*4 C2453ATGG-/-rs2472304CYP1A2*1F 34356G>AAAA+/+rs762551CYP1A2*1F C164ACAA-/-rs2069526CYP1A2*1K -739T>GGTT-/-rs56276455CYP1A2*3 D348NAGG-/-rs28399424CYP1A2*6 R431WTCC-/-rs28936700CYP1B1 10233C>TTCC-/-rs1056827CYP1B1 A119SAAA+/+rs1056836CYP1B1 L432VCGG-/-rs1800440CYP1B1 N453STTT+/+rs10012CYP1B1 R48GGGG+/+rs9282671CYP1B1 T241AAAA+/+rs1801272CYP2A6*2 A1799TTAA-/-rs35303484CYP2B6 A136GGAA-/-rs34097093CYP2B6 C1132TTCC-/-rs8192719CYP2B6 C26
MTHFRSupport Variant Report v2.7 23andMe This report is intended to translate your results into an easier to understand form. It is not intended to diagnose or treat.
Download MTHFRSupport Variant Report v2
Information
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document:
Related search queries
Guide to understanding variant classification, Variant, Phonics, Mutation or polymorphism, Creutzfeldt-Jakob Disease, Hemoglobin A1c, Variant Creutzfeldt Jakob Disease, Variant Creutzfeldt–Jakob disease, Variant intravascular large B-cell lymphoma, Intravascular large B-cell lymphoma, VARIANT II Hemoglobin, Bio-Rad Laboratories, Advanced Phonics, The Florida Center for Reading Research, Variant: Limits