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|Ambiguity code: Y
Location

This variant has not been mapped

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variant displays