Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)

Chromosome 22:35072387 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386584488, rs56939923

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad, HumanOmniExpress

About this variant

This variant overlaps 2 transcripts and has 2779 sample genotypes.

Variant displays