Original source

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

Alleles
-/T|MAF: 0.24 (T)
Location

Chromosome 8: between 23050293 and 23050294 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays