This variant maps to 7 locations

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Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name


Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 3623 sample genotypes, is associated with 7 phenotypes and is mentioned in 122 citations.

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