Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 1:153259361 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.153259361delC

Variation displays