Original source

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

Alleles
AT/-
Location

Chromosome 18:5405835-5405836 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 17 transcripts.

Variant displays