Original source

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

G/T | Ambiguity code: K | MAF: 0.40 (T)

Chromosome 6:32405921 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 5 transcripts, has 4262 sample genotypes, is associated with 3 phenotypes and is mentioned in 8 citations.

Variant displays