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Appearance - SNPedia
http://www.snpedia.com/index.php/Appearance
Visit https:/ www.reddit.com/r/SNPedia. These variations influence Skin color. One explanation for human variation at these positions is at http:/ essays.backintyme.com/item/332. Face shape 10.1371/journal.pgen.1002932. With the reference genotype rs4648477(G;G). Being 7.18x more common than the rs4648477(A;A). With the reference genotype rs4648478(C;C). Being 7.177x more common than the rs4648478(T;T). With the reference genotype rs7516150(C;C). Being 6.852x more common than the rs7516150(T;T). With the...
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Alzheimer's disease - SNPedia
http://www.snpedia.com/index.php/Alzheimer's_disease
Visit https:/ www.reddit.com/r/SNPedia. Alzheimer's, more than 150 mutations of the presenilin-1 PSEN1. And amyloid precursor protein APP. Genes have been associated with autosomally dominant inheritance (of early-onset ALZ). The most notable late-onset SNPs are. Rare 1% geno is protective. Rare 3% genotype increases risk. Rare 4% genotype doubles risk. Most genes other than ApoE. Is associated with increased risk of Alzheimer's PMID 15956169. However, according to some studies, ApoE4. SNPs are correlate...
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Recent changes - SNPedia
http://www.snpedia.com/index.php/Special:RecentChanges
Visit https:/ www.reddit.com/r/SNPedia. Track the most recent changes to the wiki on this page. This edit created a new page (also see list of new pages. This is a minor edit. This edit was performed by a bot. The page size changed by this number of bytes. Changes in last 1. Show new changes starting from 12:13, 3 September 2016. 160; 05:20 . 160; . 160; . Prev) . . Created page with { Genotype rsid=794729672 allele1=- allele2=C } ). 160; 05:19 . 160; 05:18 . 160; . 160; . Prev) . .
snpedia.com
Genotype - SNPedia
http://www.snpedia.com/index.php/Genotype
Visit https:/ www.reddit.com/r/SNPedia. As most commonly used within SNPedia, genotype. Refers to the pair of SNPs inherited at a given chromosomal position, one inherited from Dad, one inherited from Mom. Example: rs1234(A;C). Is how we indicate someone with a (A;C) genotype at snp. However, this definition of 'genotype' varies a bit from the one intended when it first introduced over 100 years ago [ 10.1126/science.35.896.340. BRCA1 (breast cancer) 5382insC. Lipoyltransferase 1 deficiency (severe).
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rs429358 - SNPedia
http://www.snpedia.com/index.php/Rs429358
Visit https:/ www.reddit.com/r/SNPedia. One of 2 snps relevant to classifying APOE genotype. 3x increased risk for Alzheimer's; 1.4x increased risk for heart disease. This SNP, located in the fourth exon of the ApoE. Gene, affects the amino acid at position 130 of the resulting protein. The more common rs429358. Allele is (T). If the allele is (C) and the same chromosome also harbors the rs7412. C) allele, the combination is known as an APOE-ε4. V3 chip) test for this SNP. Apolipoprotein E genotype is as...
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rs1815739 - SNPedia
http://www.snpedia.com/index.php/Rs1815739
Visit https:/ www.reddit.com/r/SNPedia. Better performing muscles. Likely sprinter. Mix of muscle types. Likely sprinter. Impaired muscle performance. Likely endurance athlete. Gene, encodes a premature stop codon in a muscle protein called alpha-actinin-3. The polymorphism alters position 577 of the alpha-actinin-3 protein. In the (C;C) genotype is often called RR. The truncated (T;T) is often called XX. According to [ PMID 18043716. Failed to replicate casting some doubt. T;T) The association tended th...
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Category:Is a gene - SNPedia
http://www.snpedia.com/index.php/Category:Is_a_gene
Visit https:/ www.reddit.com/r/SNPedia. This page collects all of the genes. Which actually have page text. Pages in category "Is a gene". The following 200 pages are in this category, out of 1,799 total. Previous page) ( next page. Previous page) ( next page. Retrieved from " http:/ www.snpedia.com/index.php? This page was last modified on 5 September 2011, at 21:35.
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Revised NEO Personality Inventory - SNPedia
http://www.snpedia.com/index.php/Revised_NEO_Personality_Inventory
Visit https:/ www.reddit.com/r/SNPedia. Revised NEO Personality Inventory. A list of the personality. Dimensions measured by the NEO PI-R. Including facets, is as follows:. The specific rs#s are taken from [ PMID 18957941. However many of them did not meet the p 0.05 threshold. The essential table of results is here. Retrieved from " http:/ www.snpedia.com/index.php? Title=Revised NEO Personality Inventory&oldid=465190. This page was last modified on 6 March 2012, at 12:03.
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Promethease - SNPedia
http://www.snpedia.com/index.php/Promethease
Visit https:/ www.reddit.com/r/SNPedia. The easiest way to make a report is to visit. This takes about 10 minutes and costs $5 (all major currencies and credit cards accepted. Including bitcoin and alipay). Making a Promethease report. Reading a Promethease report. Sample Promethease reports from a person tested on different 23andMe DNA chip versions:. Sample Promethease reports for another person based on data from different companies (23andMe, FamilyTreeDNA):. Read about the features. Free runs take ap...
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Category:Is a medical condition - SNPedia
http://www.snpedia.com/index.php/Category:Is_a_medical_condition
Visit https:/ www.reddit.com/r/SNPedia. Category:Is a medical condition. This page collects together medical conditions. Pages in category "Is a medical condition". The following 200 pages are in this category, out of 409 total. Previous page) ( next page. 3-Methylglutaconic aciduria type 2. Age related macular degeneration. Agenesis of the Corpus Callosum with Peripheral Neuropathy. Arrhythmogenic Right Ventricular Cardiomyopathy. Attention deficit hyperactivity disorder. Cornelia de Lange syndrome 1.
