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PGP Participant Survey
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Responses submitted 4/2/2015 21:17:20.
Show responses
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| Timestamp |
4/2/2015 21:17:20 |
| Year of birth |
1966 |
| Do you have a severe genetic disease or rare genetic trait? If so, you can add a description for your public profile. |
I have a very rare genotype, which is seen in 0% of the CEU population. I am homozygous A;A (T;T) for Rs1913474:
Rs1913474: [PMID 18636124OA-icon.png] Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma.
I have had a LOT of dental work in my day, including many fillings, crowns and bridgework with metal pins, and suspect I have a low grade lymphoma in my jawbone. I have only been diagnosed with Chronic Fatigue Syndrome (CFS) by my medical doctors, which I have had for over 15 years now.
I am curious as to whether or not this genotype is linked to CFS. |
| Sex/Gender |
Female |
| Race/ethnicity |
White |
| Maternal grandmother: Country of origin |
Finland |
| Paternal grandmother: Country of origin |
United Kingdom |
| Paternal grandfather: Country of origin |
Ireland |
| Maternal grandfather: Country of origin |
Finland |
| Month of birth |
March |
| Anatomical sex at birth |
Female |
| Maternal grandmother: Race/ethnicity |
White |
| Maternal grandfather: Race/ethnicity |
White |
| Paternal grandmother: Race/ethnicity |
White |
| Paternal grandfather: Race/ethnicity |
White |
