Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
Evidence status

HGVS names

This variant has 23 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 2770 sample genotypes.

Variant displays