Original source

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

Alleles
C/-/T | Ancestral: T
Location

Chromosome 19:5830436 (forward strand) | View in location tab

Co-located

with dbSNP rs778808 (C/T)

Most severe consequence
Evidence status

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

Variation displays