Original source

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

About this variant

This variant overlaps 5 transcripts and has 265 individual genotypes.

Variation displays