Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 12:6392000 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
HGVS name


Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 10 transcripts and has 270 sample genotypes.

Variant displays