This variant has been flagged

Variation does not map to the genome

Original source

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

Alleles
T/C/G|Ambiguity code: B|MAF: 0.01 (T)
Location

This variant has not been mapped

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 1 sample genotype.

Variant displays