Original source

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

Alleles
-/AAAC/AAACAAACAAAC
Location

Chromosome 22: between 33285624 and 33285625 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs149082037

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 1 sample genotype.

Variant displays