Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/AT
Location

Chromosome 2: between 55875126 and 55875127 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs372758243, rs57946587

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts.

Variant displays