Original source

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

Alleles
-/T/TA/TAG/TAT
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 64 HGVS names - Show

About this variant

This variant overlaps 92 transcripts.

Variant displays