Original source

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

Alleles
-/AAAGT
Location

Chromosome 19: between 33387006 and 33387007 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs143040845

This variation has 6 HGVS names - click the plus to show

Variation displays