Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.20 (G)
Location

Chromosome 14:20474292 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 10 transcripts and has 3811 sample genotypes.

Variant displays