I'm using the add-on, thanks snowathlete
Here are my results added. Inserted merylg's gene comments to save hoping back to first page of thread.
Here's are mine added. Order: 1-Lily Mendel, 2-Greg Mendel, 3-merylg, 4-Steve_22, 5-Snowathlete, 6-Roxie60
rs3176238....TT...TT... CT...CC..CT....CT
rs2302084....GG ..GG...AG...AA...AG...AG
rs2307449....GG ..GG...GT...TT...GT...GT
rs2074885.... AG...AG...GG...GG...AG...AG
rs758130......GG...GG...AG...AA...AG...AG
rs2238296....GG...GG...AG...AA...AG...AG
rs2247233....TT....TT...CT...CT...CT...CT
rs3087374...CC...AC...CC....CC....5....CC
"Mutations in the POLG gene are associated with severalmitochondrial diseases, including Alpers' disease, ataxia-neuropathy disorders, and dominant and recessive forms ofprogressive external ophthalmoplegia. A list of lists all published mutations in the POLG coding region and their associated disease can be found at the Human DNA Polymerase Gamma Mutation Database."
http://en.wikipedia.org/wiki/POLG
http://www.snpedia.com/index.php/Rs2307449
"
[PMID 16080118] Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin."
If you go into openSNP you can find the frequency of alleles & genotypes amongst openSNP users eg
http://opensnp.org/snps/rs2307449 where you can see I have the most common genotype for that snp, you the next most common & the Mendels (who we thought might be "normal"!!!) actually both have the rarest genotype!
This (first on POLG list) might be more interesting, as there is more difference in % genotype frequency:
Once again, looking at POLG gene results for 1-Lily Mendel, 2-Greg Mendel, 3-merylg, 4-steve22, 5-snowathlete, 6-roxie60
rs3087374...CC...AC...CC....CC....5....CC
http://opensnp.org/snps/rs3087374 we see that CC is common & AC is quite rare...AA would be extremely rare. Significance? "
Generally a nonpathogenic polymorphism, but may have a modifier effect that increases severity when combined in cis with other pathogenic variants."