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

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

This variant has not been mapped

Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 1 sample genotype.

Variant displays