Original source

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

Alleles
-/T | MAF: 0.03 (T)
Location

Chromosome 1: between 113849586 and 113849587 (forward strand) | View in location tab

Most severe consequence

This variation has 9 HGVS names - click the plus to show

Variation displays