Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays