phenoscanner.medschl cam.ac.uk

PhenoScanner Home Page

A database of human genotype-phenotype associations. For an example, try rs1030171. Upload a file, one rsID or hg19 chrNpos per line max 50.
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Mendelian Randomization - Home

Methods for using genetic variants in causal estimation. Next two-day course in Cambridge in Monday 26th and Tuesday 27th March 2018, research symposium Wednesday 28th March. R package for performing Mendelian randomization with summarized data is now available on CRAN. Written by Stephen Burgess and Simon G Thompson. This book gives statisticians, epidemiologists, and geneticist.

Mendelian Randomization - Home

Methods for using genetic variants in causal estimation. Next two-day course in Cambridge in Monday 26th and Tuesday 27th March 2018, research symposium Wednesday 28th March. R package for performing Mendelian randomization with summarized data is now available on CRAN. Written by Stephen Burgess and Simon G Thompson. This book gives statisticians, epidemiologists, and geneticist.

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PhenoScanner Home Page

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A database of human genotype-phenotype associations. For an example, try rs1030171. Upload a file, one rsID or hg19 chrNpos per line max 50.

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The web page had the following on the homepage, "A database of human genotype-phenotype associations." I viewed that the web site said " For an example, try rs1030171." They also said " Upload a file, one rsID or hg19 chrNpos per line max 50."

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