Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 19:17402965 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts.

Variation displays