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/T/C|Ambiguity code: H|MAF: < 0.01 (T)
Location

This variant has not been mapped

Evidence status

Synonyms

Archive dbSNP rs4483357

HGVS name

None

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant has 378 sample genotypes.

Variant displays