Original source

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

Alleles
GGGA/-
Location

Chromosome 8:118935810-118935813 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays