Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.08 (A)

Chromosome 11:17501927 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 7 transcripts, has 3760 sample genotypes and is associated with 1 phenotype.

Variant displays