Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/AT
Location

Chromosome 2: between 56102260 and 56102261 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139665854

This variation has 5 HGVS names - click the plus to show

Variation displays