Original source

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

Alleles
ATGCCTGGCTGTGTGT/-
Location

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 13 transcripts.

Variant displays