Original source

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

Alleles
-/GT | MAF: 0.02 (GT)
Location

Chromosome 8: between 127413855 and 127413856 (forward strand) | View in location tab

Most severe consequence

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

Variation displays