Original source

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

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

Chromosome 2:233403564 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.233403564G>C

Variation displays