Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: 0.02 (C)
Location

Chromosome 16:30700467 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 12 transcripts and has 2772 individual genotypes.

Variation displays