Original source

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

Alleles
T/-
Location

Chromosome 17:34355076 (forward strand) | View in location tab

Co-located

with dbSNP rs79547075 (T/C)

Most severe consequence
Evidence status

HGVS name

17:g.34355076delT

Variation displays