Original source

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

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

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

Most severe consequence
Intron variant
Evidence status

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 24 transcripts and has 3196 sample genotypes.

Variant displays