Original source

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

Alleles
-/T
Location

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

Most severe consequence
 
Intron variant

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts.

Variant displays