Original source

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

Alleles
-/GCTGCCGCCGCCGTATCCGCCGCCGGAGCT
Location

Chromosome 17: between 38975103 and 38975104 (forward strand) | View in location tab

Most severe consequence

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

Variation displays