Original source

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

Alleles
G/-
Location

Chromosome 11:18401458 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs147366647, rs111514460

This variant has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts.

Variant displays