Original source

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

Alleles
A/T | Ambiguity code: W | MAF: 0.02 (T)
Location

Chromosome 11:18400007 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

This variation has 23 HGVS names - click the plus to show

About this variant

This variant overlaps 25 transcripts and has 2541 individual genotypes.

Variation displays