Original source

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

Alleles
-/ATT
Location

Chromosome 5: between 159324095 and 159324096 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138057393

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

Variation displays