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/C/T | Ancestral: C | Ambiguity code: H
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant is associated with 6 phenotypes and is mentioned in 7 citations.

Variant displays