Original source

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

Alleles
-/T/TTA
Location

Chromosome 20: between 58671425 and 58671426 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 32 HGVS names - click the plus to show

About this variant

This variant overlaps 46 transcripts.

Variant displays