Original source

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

Alleles
AT/- | MAF: 0.12 (-)
Location

Chromosome 19:42355256-42355257 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146191696

This variation has 4 HGVS names - click the plus to show

Variation displays