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 | MAF: 0.03 (G)
Location

Chromosome 19:45418539 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 14 HGVS names - click the plus to show

Variation displays