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

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

This variant maps to 7 genomic locations; None selected

Evidence status

HGVS name

None

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 regulatory feature, has 2504 sample genotypes, is associated with 7 phenotypes and is mentioned in 121 citations.

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