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/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS name


Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant has 2505 sample genotypes, is associated with 10 phenotypes and is mentioned in 15 citations.

Variant displays