Original source

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

Alleles
-/T/TTTTT
Location

Chromosome 1: between 42828484 and 42828485 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts.

Variant displays