Original source

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

Alleles
-/AAT
Location

Chromosome 5: between 162071012 and 162071013 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts.

Variant displays