Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.09 (T)
Location

Chromosome 11:17521006 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2583 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays