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 | MAF: 0.21 (T)
Location

Chromosome 16:23182613 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23182613G>T

Variation displays