Original source

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

Alleles
-/AAAC | MAF: 0.05 (AAAC)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144761404

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

Variation displays