Original source

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

-/ACCT | MAF: 0.02 (AGGT)

Chromosome 1: between 149033254 and 149033255 (forward strand) | View in location tab

Most severe consequence

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

About this variant

This variant overlaps 13 transcripts and has 1092 individual genotypes.

Variation displays