This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A | Ancestral: C | Ambiguity code: M

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 1 regulatory feature, is associated with 6 phenotypes and is mentioned in 5 citations.

Variant displays