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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.29 (T)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

This variant has 4 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant has 2514 sample genotypes.

Variant displays