Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.46 (C)
Location

Chromosome 11:112050384 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 5 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts and has 2588 sample genotypes.

Variant displays