Original source

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

Alleles
-/T
Location

Chromosome 1: between 26792321 and 26792322 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

Variation displays