Original source

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

Alleles
AAG/- | MAF: 0.24 (-)
Location

Chromosome 11:114079112-114079114 (forward strand) | View in location tab

Most severe consequence

This variation has 5 HGVS names - click the plus to show

Variation displays