Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.23 (C)
Location

Chromosome 11:66238852 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2546 sample genotypes and is associated with 1 phenotype.

Variant displays