This variant maps to 2 locations

Select a location:
Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs17712822, rs59569355

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human660W-quad

About this variant

This variant overlaps 1 regulatory feature and has 2849 sample genotypes.

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