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ANMERKUNG: Ausgelagert ab hier https://www.symptome.ch/threads/methylierungszyklus-es-geht-mir-besser.98892/page-83#post-1021881
AO
Da CFS fast immer mit SD-Unterfunktion einhergeht mal jenes von 23andme:
https://www.23andme.com/about/factoids/
AO
Da CFS fast immer mit SD-Unterfunktion einhergeht mal jenes von 23andme:
JUNE 2011
New genetic factors for hypothyroidism
Our research data suggests two novel connections between genetics and hypothyroidism, a condition that affects about 5% of the population, especially women over the age of 50. Hide Details «
DETAILS
With the help of our research participants, we have identified several genetic variants that may be associated with risk for hypothyroidism in individuals with European ancestry. The SNPs rs965513 in the FOXE1 gene and rs2476601 in the PTPN22 gene have already been reported in studies of thyroid function or thyroid disease. Two other associations are completely novel — the C version of rs4915077 in the VAV3 gene is associated with slightly higher odds of hypothyroidism based on our research data, while the T version of rs3184504 in the SH2B3 gene appears to have a slightly protective effect. Many of these genes are involved in the immune system.
23andMe research - frequency of thyroid disorders
23andMe Research customer survey data
REFERENCE
Eriksson N et al. (2012) Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci. PLoS ONE 7(4): e34442.
https://www.23andme.com/about/factoids/
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