Original source

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

-/AGAC | MAF: 0.20 (-)

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

Most severe consequence
Evidence status


Archive dbSNP rs139940528

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

About this variant

This variant overlaps 12 transcripts and has 1093 individual genotypes.

Variation displays