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
A/G|Ambiguity code: R|MAF: 0.46 (C)
Location

This variant has not been mapped

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant has 1259 sample genotypes.

Variant displays