Original source

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

Alleles
-/GGAA
Location

Chromosome 14: between 104784033 and 104784034 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147782193

This variation has 9 HGVS names - click the plus to show

Variation displays