This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
G/C/T|Ambiguity code: B
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

This variant has 11 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant has 2 sample genotypes.

Variant displays