Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
HGVS name

12:g.6392000G>T

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays