Original source

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

Alleles
-/G
Location

Chromosome 1: between 145928620 and 145928621 (forward strand) | View in location tab

Most severe consequence

This variation has 15 HGVS names - click the plus to show

Variation displays