Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:48922027 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

8:g.48922027G>T

Variation displays