Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.22 (A)
Location

Chromosome 11:116836867 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 3691 sample genotypes and is mentioned in 1 citation.

Variant displays