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 6:52419101 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.52419101A>C

Variation displays