Original source

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

Alleles
-/TT
Location

Chromosome 2: between 55888335 and 55888336 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs369111970, rs575804182

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays