Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.06 (G)

Chromosome 11:44595279 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386619698

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 12 transcripts and has 2778 sample genotypes.

Variant displays