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 2:232539308 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.232539308A>C

Variation displays