Original source

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

Alleles
TAA/- | MAF: 0.47 (-)
Location

Chromosome 20:58671478-58671480 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 16 HGVS names - click the plus to show

Variation displays