Original source

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

Alleles
-/ATTATT
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs398121053

HGVS names

This variant has 3 HGVS names - Show

About this variant

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

Variant displays