Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (A)

Chromosome 11:34533644 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59570632, rs386616866

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 1 transcript, has 3809 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays