Original source

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

Alleles
-/AA | MAF: 0.37 (-)
Location

Chromosome 1: between 225409160 and 225409161 (forward strand) | View in location tab

Most severe consequence

This variation has 4 HGVS names - click the plus to show

Variation displays