Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)

Chromosome 11:2160013 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 13 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays