Original source

Variants (including SNPs and indels) imported from dbSNP (release 136) | [View in dbSNP]

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

Chromosome 4:80833674 (forward strand) | View in location tab

Most severe consequence
HGVS name

4:g.80833674A>C

Variation displays