This variant maps to 7 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

This variant maps to 7 genomic locations; None selected

Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant is associated with 14 phenotypes and is mentioned in 1 citation.

Variant displays