Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.38 (T)
Location

Chromosome 19:48978948 (forward strand) | View in location tab

Co-located

with dbSNP rs67939886 (AT/GA)

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Variation displays