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Integrate dbSNP for variant interpretation #3

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mattmight opened this issue Jan 19, 2018 · 1 comment
Open

Integrate dbSNP for variant interpretation #3

mattmight opened this issue Jan 19, 2018 · 1 comment

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@mattmight
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https://www.ncbi.nlm.nih.gov/snp/

@andrewsu
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Many (most?) annotations of human genetic variants can be accessed programmatically through myvariant.info. Happy to walk you through usage, and let me know if there's an annotation resource that's not there...

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