Original source

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

Alleles
-/A|MAF: 0.11 (A)
Location

Chromosome 2: between 219252541 and 219252542 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56732349, rs138627203

HGVS names

This variant has 11 HGVS names - Show

About this variant

Variant displays