Original source

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

Alleles
-/T
Location

Chromosome 1: between 26792338 and 26792339 (forward strand)|View in location tab

Co-located variant

dbSNP rs397718823 (-/T)

Most severe consequence
 
Intron variant
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays