Original source

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

Alleles
C/T | Ancestral: A | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 16:30756019 (forward strand) | View in location tab

Most severe consequence
Evidence status

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 24 transcripts and has 3196 individual genotypes.

Variation displays