Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
TT/-
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369111970

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

Variation displays