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 | MAF: < 0.01 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant has 2504 sample genotypes, is associated with 6 phenotypes and is mentioned in 2 citations.

Variant displays