Original source

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

Alleles
ATTT/-
Location

Chromosome 18:44751575-44751578 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs68057386, rs144397762

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

Variation displays