Original source

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

Alleles
AT/- | MAF: 0.39 (AT)
Location

Chromosome 13:19962497-19962498 (forward strand) | View in location tab

Most severe consequence

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

Variation displays