Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R
Location

Chromosome 14:28766943 (forward strand) | View in location tab

Most severe consequence
HGVS name

14:g.28766943G>A

Variation displays