Original source

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

Alleles
-/GCTGCCGCCGCCGTATCCGCCGCCGGAGCT
Location

Chromosome 17: between 40818851 and 40818852 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Variation displays