Original source

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

Alleles
ATGCCTGGCTGTGTGT/-
Location

Chromosome 18:5469447-5469462 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts.

Variant displays