Original source

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

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 26 transcripts.

Variant displays