Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.19 (T)
Location

Chromosome 14:100839783 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60864218, rs17810418

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

Variant displays