This variant has been flagged

Variation has more than 3 different alleles

Original source

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

A/C/G/T | Ambiguity code: N | MAF: 0.14 (C)

Chromosome 6:32643199 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 15 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts and has 2506 sample genotypes.

Variant displays