Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/-
Location

Chromosome 11:18400461 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 25 transcripts.

Variant displays