Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 16:30697197 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.30697197A>C

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays