Original source

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

Alleles
-/TAAT | MAF: 0.09 (TAAT)
Location

Chromosome 19: between 33387165 and 33387166 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs141718354

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

Variation displays