Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 1:75127234 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.75127234C>G

Variation displays