Original source

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

Alleles
ATTT/-
Location

Chromosome 18:44751575-44751578 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs68057386, rs144397762

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays