Original source

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

Alleles
-/AT/ATAT|MAF: 0.50 (-)
Location

Chromosome 10: between 48405106 and 48405107 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 24 HGVS names - Show

About this variant

Variant displays