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
A/T/C/G | Ambiguity code: N
Location

This variation has not been mapped

Evidence status

Synonyms

Archive dbSNP rs117230199, rs17663768

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant has 1057 individual genotypes.

Variation displays