Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.49 (A)

Chromosome 20:9368386 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59506618, rs3761166

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3766 sample genotypes and is associated with 1 phenotype.

Variant displays