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The SNP variants that are associated with Wilson's disease should have increased magnitude. I don't know how the mutations the studies mentions correspond to dbSNPs.

Here's one way you could look up the correspondence for at least some of the variants ... go to OMIM, search for the Wilson disease page, see that it refers to the ATP7B gene entry, so go there and then either scroll down to the allele section, or, jump to the Table View of allelic variants.Greg (talk) 14:38, 14 April 2014 (UTC)