Original source

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

Alleles
-/C
Location

Chromosome 17: between 15239508 and 15239509 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB NM_000304.2:c.281dupG, NM_000304.2:c.281_282insG

This variation has 18 HGVS names - click the plus to show

Variation displays