This variant maps to 7 locations

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Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.44 (T)

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name


This variant has assays on 11 chips - click the plus to show

About this variant

This variant has 2508 sample genotypes, is associated with 7 phenotypes and is mentioned in 5 citations.

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