Original source

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

Alleles
-/ATTATT
Location

Chromosome 19: between 48978553 and 48978554 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs398121053

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

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 3 sample genotypes.

Variant displays