Original source

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

Alleles
-/T
Location

Chromosome 8: between 118927569 and 118927570 (forward strand)|View in location tab

Co-located variant

dbSNP rs397706964 (-/T)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays