This variant has been flagged

  • None of the variant alleles match the reference allele
  • Variation has more than 3 different alleles
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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C/G/T|Ancestral: A|Ambiguity code: N
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

This variant has 5 synonyms - Show

HGVS name

None

About this variant

This variant has 12 sample genotypes.

Variant displays