Talk:ClinVar
From SNPedia
Rs11209026 the risk has a Good repute, but Significance = 255 usually indicates a flip and we avoid setting the geno for that reason.
Rs11203289 might have been autoflagged as of notable risk, but seems inconsequential.
Rs1801265 risk allele is more common
Rs2476601 but the page text mentions a flip between some platforms
Rs505151 but was set to significance=2
test case for multi-nucleotide with overlapping chars
multiple alleles
Rs80356760 Pathlogical allele char combination
Rs1061170 longevity vs AMD?
Rs121912698 something wrong with info link
Rs76914770 boring for now, due to Disease=OMIM + Significance=255.
Rs1494555 literature + rare in hapmap
