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

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB 13830

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant is associated with 6 phenotypes and is mentioned in 1 citation.

Variant displays