Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:158420876 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.158420876A>C

Variation displays