Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.37 (A)
Location

Chromosome 11:18399905 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

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

About this variant

This variant overlaps 25 transcripts and has 2510 sample genotypes.

Variant displays