This variation maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

This variation maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant has 262 individual genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays