Original source

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

Alleles
-/GT|MAF: 0.02 (GT)
Location

Chromosome 8: between 127413855 and 127413856 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays