ThyroStabilityGS

Gene Savvy ThyroStabilityGS 0 stars, based on 0 reviews 0 5
$750.00

ThyroStabilityGS

0 Reviews
$750.00
ThyroStabilityGS

ThyroStabilityGS

$750.00
Model Number: 000106GS

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750.000
Categories: , Specific Affliction
Manufacturer: Gene Savvy
  • Description
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Panel Overview. The ThyroStabilityGS is a unique genetic sequencing service that looks at genes associated with thyroid dysregulation, such as abnormal thyroid hormone metabolism, hypothyroidism, thyroid hypoplasia, thyroid dyshormonogenesis, and others. We take a novel approach by providing several types of clinical data for your healthcare professional to evaluate. We perform exon region gene sequencing for over 25 genes related to thyroid dysregulation, as well as looking at over 15 single locations (SNVs) related to thyroid dysregulation, plus another 75 single locations (SNPs) related to general wellness. The ThyroStabilityGS Panel is performed using the latest next-generation DNA sequencing technology.

Gene List.    

Disease-related Full Gene Sequencing List: ALB, CTLA4, DUOX2, DUOXA2, FOXE1, GNAS, IGSF1, IYD, NKX2-1, NKX2-5, PAX8, POU1F1, PROP1, SECISBP2, SERPINA7, SLC16A2, SLC26A4, SLC5A5, TG, THRA, THRB, TPO, TRHR, TSHB, TSHR, TTR

Disease-related SNV List: CAPZB, CD40, CTLA4+, DIO1, DIO2+, FCRL3+, FOXE1, FOXP3+, IFNG+, ITPR3, PDE8B+, SCGB3A2, SLCO1C1

General Wellness SNP List: AANAT, ACAT1, ACE, ADM, AHCY+, BDNF, BHMT+, BTD, C5, CBS+, COMT+, CoQ2, CoQ3, COX5A, COX6C, CYP27A1, ENPP1, GSS, GSTM1, GSTP+, IGF1, IL10, IL23R, IL6, IL6R, KCNJ11, MAOA, MAOB, MAT1A, MAT2B, MTHFR+, MTR, MTRR+, NOS, NOS3, PDHA1, PDHB, PNMT, PTPN22, PTS, QDPR, SHMT1, SIRT1, SLC22A5, SLC25A15, SLC25A32, SLC2A1, SOD2, SUOX+, TGFB1+, TNF+, TRAF1, TRAP1, USF1, VDR+

Panel Performance. 

This test was designed to sequence the exons and canonical splice sites (+/1,2) of a panel of genes associated with the clinical management and actionable treatment options of common Thyroid Dis-regulation symptoms. These genetic variants can be associated with functional disturbance, pathways involved and targetable action to facilitate improved function and epigenetic outcomes. GeneSavvy has developed highly advanced protocols to target and extract variants in exonic regions, intronic regions of interest, splice sites, and untranslated gene regions of interest with the following technical specifications:

  • Mean Depth of Coverage: 50x
  • Specificity: >98%
  • Sensitivity: >94%

 

*All GeneSavvy Genetic tests must be signed for by a physician. If you don’t currently have a physician, we can connect you with a physician after you complete your order to review your health information and submit the needed documents.

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