Original source

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

C/T | Ambiguity code: Y | MAF: 0.37 (C)

Chromosome 11:2307718 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3782054

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 17 transcripts and has 2513 sample genotypes.

Variant displays