Original source

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

Alleles
T/A/G | Ancestral: G | Ambiguity code: D | MAF: 0.14 (G)
Location

Chromosome 11:72238968 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 23 transcripts and has 2504 individual genotypes.

Variation displays