Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 14:100829164 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 25 transcripts and has 261 sample genotypes.

Variant displays