This variation has been flagged

Variation does not map to the genome

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

This variation has not been mapped

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays