Original source

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

Alleles
-/GTG/GTGTGT
Location

Chromosome 10: between 48403958 and 48403959 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 24 HGVS names - click the plus to show

Variation displays