Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.01 (G)
Location

Chromosome 6:52419426 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.52419426A>G

Variation displays