This variant has been flagged

None of the variant alleles match the reference allele

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Original source

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

T/A | Ancestral: A | Ambiguity code: W

This variant maps to 2 genomic locations; None selected

Evidence status

HGVS name


About this variant

This variant has 2 sample genotypes.

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