Original source

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

G/A | Ambiguity code: R | MAF: 0.16 (A)

Chromosome 20:5310688 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays