This variant maps to 2 locations

Select a location:
Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant has 262 sample genotypes, is associated with 4 phenotypes and is mentioned in 2 citations.

Variant displays