Original source

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

G/C/T | Ancestral: G | Ambiguity code: B | MAF: 0.01 (C)

Chromosome 11:27656953 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 56 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 54 transcripts and has 2504 sample genotypes.

Variant displays