Original source

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

Alleles
-/AGAC | MAF: 0.20 (-)
Location

Chromosome 4: between 174515617 and 174515618 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139940528

This variation has 13 HGVS names - click the plus to show

Variation displays