Original source

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

Alleles
GT/-
Location

Chromosome 8:42482738-42482739 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts.

Variant displays