This variant has been flagged

  • None of the variant alleles match the reference allele
  • Mapped position is not compatible with reported alleles
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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

A/C | Ambiguity code: M

This variant maps to 2 genomic locations; None selected

HGVS name


About this variant

This variant overlaps 1 regulatory feature.

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