Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.44 (C)

Chromosome 11:17521325 (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 12 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 16 transcripts, has 4032 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays