Original source

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

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

Chromosome 12:20833670-20833671 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs140550860

This variation has 6 HGVS names - click the plus to show

Variation displays