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Why does dbSNP refer to an A/G variation in the sequence and ancestral description of rs2476601, when several reference publications indicate that it is a 1858C>T polymorphism?

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Why does dbSNP refer to an A/G variation in the sequence and ancestral description of rs2476601, when several reference publications indicate that it is a 1858C>T polymorphism?

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The alleles for rs1611430 are reported A/G/T, yet the variation class is SNP. I thought this classification was reserved for biallelic SNPs, and that tri- and multi-alleles were classified as MNPs.

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