Original source

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

Alleles
-/ATT
Location

Chromosome 5: between 159324096 and 159324097 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and 1 regulatory feature.

Variant displays