Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 11 transcripts, has 2571 individual genotypes and is mentioned in 1 citation.

Variation displays