Original source

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

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

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


with dbSNP rs67939886 (AT/GA)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 6 transcripts and has 1108 individual genotypes.

Variation displays