Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.35 (T)
Location

Chromosome 14:100835874 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 24 transcripts and has 2507 sample genotypes.

Variant displays