This variant maps to 2 locations

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Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.01 (G)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

HGVS name

None

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 1 regulatory feature, has 2560 sample genotypes, is associated with 4 phenotypes and is mentioned in 3 citations.

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