Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 8 HGVS names - click the plus to show

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 2583 sample genotypes and is associated with 2 phenotypes.

Variant displays