This variant has been flagged

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
C/A/G/T|Ambiguity code: N|MAF: 0.24 (T)
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

This variant has 8 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant has 2516 sample genotypes.

Variant displays