Original source

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

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

Chromosome 6:52283899 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.52283899A>C

Variation displays