Original source

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

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

Chromosome 14:100826079 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays