Original source

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

-/AAAC | MAF: 0.05 (AAAC)

Chromosome 22: between 33282360 and 33282361 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs144761404

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 1093 individual genotypes.

Variation displays