Original source

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

Alleles
AAAC/- | MAF: 0.36 (AAAC)
Location

Chromosome 11:18405840-18405843 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs148072862, rs143718787

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

Variation displays